Processingenjör - Lediga jobb

Silex Microsystems is the world’s leading pure-play MEMS foundry, customizing solutions for prominent global clients in industries such as pharmaceuticals, consumer electronics, and automotive. We’re now growing more than ever, and are expanding our Manufacturing organization with new Process Engineer positions in several areas.

Read more about Silex here.

The Area

The area consists of a team of both engineers and service technicians where collaboration is critical to ensure good process stability, tool up-time and continuous improvement. All Process Engineers report to the Area Manager in their area.

Wet

• A fast-paced, varied and unique area where the processes differ a lot: wet-etching, deposition and vapor techniques are used to both remove and build material on our chips. The team consists of five Service Technicians and ten Process Engineers.

The role

Your overall responsibility is to ensure manufacturing goals are met, together with operators and service technicians. Your days will be a mix of meetings with Product Managers and developing new processes that meet customers' specifications.

You will also participate in creating work routines for operators and solving problems that occur in the area, driving improvement projects to enhance our workflow and processes in the area.

In this role, you will:

• Develop, maintain and improve processes.

• Handle stopped production batches and development material together with process integration engineers (PIs).

• Be a part of creating/improving the infrastructure for operator training and make sure current routine is available and up to date.

• Participate in process qualification of new equipment/materials and release to them production.

• Participate in the startup of new products, review specifications and process flows.

• Grow into taking responsibility for area equipment, improving the tool uptime, maintain and develop new standardized process modules.

• Drive improvement projects independently.

We are looking for someone who has

• A master's degree in engineering, specializing in Applied Physics, Chemical Engineering, Material Science, or a related field.

• At least one year of experience in an engineering role, preferably in production/development environments.

• The ability to see opportunities for improvement and manage projects to follow through with those improvements in a proactive way.

• Strong problem-solving skills and the ability to work effectively in a team environment.

• Strong skills in documentation and quality management.

• Excellent communication skills in English; proficiency in Swedish is considered a merit.

What we offer you

• An opportunity to work closely with talented and inspiring colleagues in a collaborative environment.

• A chance to be part of a world-leading company, driving the future of MEMS technology.

• The ability to engage with cutting-edge innovations that shape global industries and everyday life.

• The satisfaction of contributing directly to transformative technologies at the industry’s most advanced pure-play MEMS foundry.

About Silex

Sweden’s Silex Microsystems manufactures mechanical and electrical systems in micro scale, in the form of MEMS chips. MEMS technology makes it possible to produce pressure sensors that are small enough to be injected into the human bloodstream. Silex was founded in 2000, and now has an annual turnover of approximately SEK 1 billion and 350 employees. With around 80 active customers globally, Silex is one of the world’s leading independent MEMS manufacturers.

The recruitment process

Due to the summer holiday period, the recruitment process will be temporarily paused until mid-to-late August. In the meantime, we encourage you to apply by attaching your CV or LinkedIn profile, and answering a few questions. You do not need to write a cover letter.

Our recruitment process is designed to ensure a fair and objective assessment. If you progress through the process, you will first complete a personality and logical assessment, followed by a digital interview with a Talent Acquisition Partner. Next, you will meet with the Area Manager for an in-person Hiring Manager interview, and finally with our VP of Manufacturing for a concluding interview.

Before an offer, we also conduct reference checks, a background check, and a drug test. Randomized alcohol- and drug testing is conducted for all of our employees during employment.

Silex Microsystems is the world’s leading pure-play MEMS foundry, customizing solutions for prominent global clients in industries such as pharmaceuticals, consumer electronics, and automotive. We’re now growing more than ever, and are expanding our Manufacturing organization with new Process Engineer positions in several areas.

Read more about Silex here.

The Area

The area consists of a team of both engineers and service technicians where collaboration is critical to ensure good process stability, tool up-time and continuous improvement. All Process Engineers report to the Area Manager in their area.

Wet

• A fast-paced, varied and unique area where the processes differ a lot: wet-etching, deposition and vapor techniques are used to both remove and build material on our chips. The team consists of five Service Technicians and ten Process Engineers.

The role

Your overall responsibility is to ensure manufacturing goals are met, together with operators and service technicians. Your days will be a mix of meetings with Product Managers and developing new processes that meet customers' specifications.

You will also participate in creating work routines for operators and solving problems that occur in the area, driving improvement projects to enhance our workflow and processes in the area.

In this role, you will:

• Develop, maintain and improve processes.

• Handle stopped production batches and development material together with process integration engineers (PIs).

• Be a part of creating/improving the infrastructure for operator training and make sure current routine is available and up to date.

• Participate in process qualification of new equipment/materials and release to them production.

• Participate in the startup of new products, review specifications and process flows.

• Grow into taking responsibility for area equipment, improving the tool uptime, maintain and develop new standardized process modules.

• Drive improvement projects independently.

We are looking for someone who has

• A master's degree in engineering, specializing in Applied Physics, Chemical Engineering, Material Science, or a related field.

• At least one year of experience in an engineering role, preferably in production/development environments.

• The ability to see opportunities for improvement and manage projects to follow through with those improvements in a proactive way.

• Strong problem-solving skills and the ability to work effectively in a team environment.

• Strong skills in documentation and quality management.

• Excellent communication skills in English; proficiency in Swedish is considered a merit.

What we offer you

• An opportunity to work closely with talented and inspiring colleagues in a collaborative environment.

• A chance to be part of a world-leading company, driving the future of MEMS technology.

• The ability to engage with cutting-edge innovations that shape global industries and everyday life.

• The satisfaction of contributing directly to transformative technologies at the industry’s most advanced pure-play MEMS foundry.

About Silex

Sweden’s Silex Microsystems manufactures mechanical and electrical systems in micro scale, in the form of MEMS chips. MEMS technology makes it possible to produce pressure sensors that are small enough to be injected into the human bloodstream. Silex was founded in 2000, and now has an annual turnover of approximately SEK 1 billion and 350 employees. With around 80 active customers globally, Silex is one of the world’s leading independent MEMS manufacturers.

The recruitment process

Due to the summer holiday period, the recruitment process will be temporarily paused until mid-to-late August. In the meantime, we encourage you to apply by attaching your CV or LinkedIn profile, and answering a few questions. You do not need to write a cover letter.

Our recruitment process is designed to ensure a fair and objective assessment. If you progress through the process, you will first complete a personality and logical assessment, followed by a digital interview with a Talent Acquisition Partner. Next, you will meet with the Area Manager for an in-person Hiring Manager interview, and finally with our VP of Manufacturing for a concluding interview.

Before an offer, we also conduct reference checks, a background check, and a drug test. Randomized alcohol- and drug testing is conducted for all of our employees during employment.

Silex Microsystems is the world’s leading pure-play MEMS foundry, customizing solutions for prominent global clients in industries such as pharmaceuticals, consumer electronics, and automotive. We’re now growing more than ever, and are expanding our Manufacturing organization with new Process Engineer positions in several areas.

Read more about Silex here.

The Area

The area consists of a team of both engineers and service technicians where collaboration is critical to ensure good process stability, tool up-time and continuous improvement. All Process Engineers report to the Area Manager in their area.

Wet

• A fast-paced, varied and unique area where the processes differ a lot: wet-etching, deposition and vapor techniques are used to both remove and build material on our chips. The team consists of five Service Technicians and ten Process Engineers.

The role

Your overall responsibility is to ensure manufacturing goals are met, together with operators and service technicians. Your days will be a mix of meetings with Product Managers and developing new processes that meet customers' specifications.

You will also participate in creating work routines for operators and solving problems that occur in the area, driving improvement projects to enhance our workflow and processes in the area.

In this role, you will:

• Develop, maintain and improve processes.

• Handle stopped production batches and development material together with process integration engineers (PIs).

• Be a part of creating/improving the infrastructure for operator training and make sure current routine is available and up to date.

• Participate in process qualification of new equipment/materials and release to them production.

• Participate in the startup of new products, review specifications and process flows.

• Grow into taking responsibility for area equipment, improving the tool uptime, maintain and develop new standardized process modules.

• Drive improvement projects independently.

We are looking for someone who has

• A master's degree in engineering, specializing in Applied Physics, Chemical Engineering, Material Science, or a related field.

• At least one year of experience in an engineering role, preferably in production/development environments.

• The ability to see opportunities for improvement and manage projects to follow through with those improvements in a proactive way.

• Strong problem-solving skills and the ability to work effectively in a team environment.

• Strong skills in documentation and quality management.

• Excellent communication skills in English; proficiency in Swedish is considered a merit.

What we offer you

• An opportunity to work closely with talented and inspiring colleagues in a collaborative environment.

• A chance to be part of a world-leading company, driving the future of MEMS technology.

• The ability to engage with cutting-edge innovations that shape global industries and everyday life.

• The satisfaction of contributing directly to transformative technologies at the industry’s most advanced pure-play MEMS foundry.

About Silex

Sweden’s Silex Microsystems manufactures mechanical and electrical systems in micro scale, in the form of MEMS chips. MEMS technology makes it possible to produce pressure sensors that are small enough to be injected into the human bloodstream. Silex was founded in 2000, and now has an annual turnover of approximately SEK 1 billion and 350 employees. With around 80 active customers globally, Silex is one of the world’s leading independent MEMS manufacturers.

The recruitment process

Due to the summer holiday period, the recruitment process will be temporarily paused until mid-to-late August. In the meantime, we encourage you to apply by attaching your CV or LinkedIn profile, and answering a few questions. You do not need to write a cover letter.

Our recruitment process is designed to ensure a fair and objective assessment. If you progress through the process, you will first complete a personality and logical assessment, followed by a digital interview with a Talent Acquisition Partner. Next, you will meet with the Area Manager for an in-person Hiring Manager interview, and finally with our VP of Manufacturing for a concluding interview.

Before an offer, we also conduct reference checks, a background check, and a drug test. Randomized alcohol- and drug testing is conducted for all of our employees during employment.

Silex Microsystems is the world’s leading pure-play MEMS foundry, customizing solutions for prominent global clients in industries such as pharmaceuticals, consumer electronics, and automotive. We’re now growing more than ever, and are expanding our Manufacturing organization with new Process Engineer positions in several areas.

Read more about Silex here.

The Area

The area consists of a team of both engineers and service technicians where collaboration is critical to ensure good process stability, tool up-time and continuous improvement. All Process Engineers report to the Area Manager in their area.

Wet

• A fast-paced, varied and unique area where the processes differ a lot: wet-etching, deposition and vapor techniques are used to both remove and build material on our chips. The team consists of five Service Technicians and ten Process Engineers.

The role

Your overall responsibility is to ensure manufacturing goals are met, together with operators and service technicians. Your days will be a mix of meetings with Product Managers and developing new processes that meet customers' specifications.

You will also participate in creating work routines for operators and solving problems that occur in the area, driving improvement projects to enhance our workflow and processes in the area.

In this role, you will:

• Develop, maintain and improve processes.

• Handle stopped production batches and development material together with process integration engineers (PIs).

• Be a part of creating/improving the infrastructure for operator training and make sure current routine is available and up to date.

• Participate in process qualification of new equipment/materials and release to them production.

• Participate in the startup of new products, review specifications and process flows.

• Grow into taking responsibility for area equipment, improving the tool uptime, maintain and develop new standardized process modules.

• Drive improvement projects independently.

We are looking for someone who has

• A master's degree in engineering, specializing in Applied Physics, Chemical Engineering, Material Science, or a related field.

• At least one year of experience in an engineering role, preferably in production/development environments.

• The ability to see opportunities for improvement and manage projects to follow through with those improvements in a proactive way.

• Strong problem-solving skills and the ability to work effectively in a team environment.

• Strong skills in documentation and quality management.

• Excellent communication skills in English; proficiency in Swedish is considered a merit.

What we offer you

• An opportunity to work closely with talented and inspiring colleagues in a collaborative environment.

• A chance to be part of a world-leading company, driving the future of MEMS technology.

• The ability to engage with cutting-edge innovations that shape global industries and everyday life.

• The satisfaction of contributing directly to transformative technologies at the industry’s most advanced pure-play MEMS foundry.

About Silex

Sweden’s Silex Microsystems manufactures mechanical and electrical systems in micro scale, in the form of MEMS chips. MEMS technology makes it possible to produce pressure sensors that are small enough to be injected into the human bloodstream. Silex was founded in 2000, and now has an annual turnover of approximately SEK 1 billion and 350 employees. With around 80 active customers globally, Silex is one of the world’s leading independent MEMS manufacturers.

The recruitment process

Due to the summer holiday period, the recruitment process will be temporarily paused until mid-to-late August. In the meantime, we encourage you to apply by attaching your CV or LinkedIn profile, and answering a few questions. You do not need to write a cover letter.

Our recruitment process is designed to ensure a fair and objective assessment. If you progress through the process, you will first complete a personality and logical assessment, followed by a digital interview with a Talent Acquisition Partner. Next, you will meet with the Area Manager for an in-person Hiring Manager interview, and finally with our VP of Manufacturing for a concluding interview.

Before an offer, we also conduct reference checks, a background check, and a drug test. Randomized alcohol- and drug testing is conducted for all of our employees during employment.

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se

Bohus Biotech is an innovative company focused on the development and manufacture of high-quality products containing hyaluronic acid (HA). We are now in an expansive phase, investing in the products and processes of the future. We are looking for a driven Process Engineer who wants to become part of Bohus’s future and contribute to the continued development of hyaluronic acid and its products.

As our Process Engineer, you will be responsible for developing, optimizing, validating, and maintaining manufacturing processes to ensure product quality, process robustness, regulatory compliance, and operational efficiency. The role supports both existing production processes and the introduction of new products and technologies. You will be working closely with dedicated and highly competent colleagues within Production, Quality Assurance, Regulatory Affairs, Supply Chain, and R&D. You will get the exciting opportunity to build, shape and optimize our processes and apply your experience and expertise to ensure the highest manufacturing standards. If this sounds interesting to you - Come join us!

This is a full-time position and based in our company location in Strömstad, Sweden. On-site in Strömstad preferred, but hybrid solutions are possible for the right candidate. We will interview candidates continuously and welcome your application today.

The Process Engineer is responsible for ensuring that manufacturing processes are robust, efficient, validated, and compliant throughout the product lifecycle. You will bridge day-to-day manufacturing support with longer-term process development and operational excellence initiatives. The position reports to the COO.

Duties and responsibilities include:

• Develop, implement, and continuously improve manufacturing processes to enhance quality, yield, and efficiency.

• Lead root cause investigations and implement corrective and preventive actions (CAPA).

• Plan, execute, and document validation activities, including Process Validation, Equipment Qualification (IQ/OQ/PQ), Cleaning Validation, and Test Method Validation/Verification.

• Provide technical support to production, investigating process deviations, non-conformities, and out-of-specification results.

• Lead continuous improvement initiatives using structured problem-solving methods such as Root Cause Analysis, FMEA, and 5 Why.

• Ensure processes comply with ISO 13485, EU MDR 2017/745, ISO 14971, and GMP principles.

• Support audits and inspections by customers, regulatory authorities, and Notified Bodies.

• Support technology transfers from R&D to production and participate in cross-functional development projects.

• Approve process validation documentation according to delegated authority and escalate process risks impacting product quality, compliance, or supply.

The suitable candidate has the following qualifications:

• Formal academic degree level (BSc. or MSc.) in chemical engineering, biotechnology, pharmaceutical science or related.

• Strong background in process engineering preferably combined with validation engineering experience.

• Experience working in a manufacturing environment within a regulated industry (e.g. Medical Devices, Pharmaceuticals, Biotechnology, or other regulated industries).

• Experience with process optimization, process validation and problem solving.

• Experience with sterile processes, equipment qualification (IQ, OQ, PQ), process validation, troubleshooting, and continuous improvement would be highly valuable.

• Experience working with Quality Management Systems.

• Knowledge of statistical analysis and process capability concepts.

• Excellent communication and documentation skills in English are required

The successful candidate for this position will be someone who:

• Has a strong technical and analytical mindset.

• Enjoys solving complex manufacturing and process-related challenges.

• Is structured and detail-oriented.

• Takes ownership and drives improvements independently.

• Communicates effectively across departments and organizational levels.

• Combines hands-on problem solving with a systematic approach.

• Thrives in a fast-paced environment where quality, compliance, and operational performance are equally important.

We offer a dynamic working environment with significant opportunity to make an impact — contributing to Bohus’s success as well as your own growth and development.

Founded in 1993, BOHUS has been at the forefront of Hyaluronic Acid (HA) development and manufacturing for over three decades. Our journey began with a vision to revolutionize the HA industry through innovation and commitment to excellence.

With more than 30 years of expertise, the company has established a strong international presence with products distributed to hospitals, clinics, and physicians in over 60 countries worldwide.

Bohus Biotech focuses exclusively on high quality hyaluronic acid technologies across three therapeutic areas:

• Ophthalmology – OVD solutions supporting tissue protection during cataract surgery

• Aesthetics – Dermal fillers based on the proprietary SHAPE™ technology platform

• Orthopaedics – Injectable treatments for osteoarthritis

All research, development, and manufacturing are located in Strömstad, Sweden, ensuring full control over product quality and innovation. For more information, visit the company's web sites at: www.bohusbiotech.com

Krishan Johansson Haque, PhD

Sr Recruitment Consultant, QRIOS Life Science & Engineering

T: +46 (0)72-070 16 53

E: krishan.johansson-haque@qrios.se