Biomanufacturing Technician

Warker LLC; Portsmouth (NH); On-site; USD 65,000 - 90,000; Full time

Job summary

Warker LLC in New Hampshire is seeking a Manufacturing Biotechnologist 1 to execute cGMP biopharmaceutical manufacturing activities, supporting upstream and downstream operations in a highly regulated environment. You will work closely with cross-functional teams to ensure safety, product quality, and on-time delivery.

Responsibilities include running bioreactor operations, clarification, chromatography and filtration; performing in-process sampling and basic analytical testing; maintaining

Qualifications

• Knowledge of cGMP manufacturing and compliance expectations.
• Hands-on experience with bioprocess unit operations (e.g., bioreactors, chromatography, filtration).
• Ability to perform routine sampling and basic analytical testing.
• Strong attention to detail for batch record accuracy and documentation.
• Team-oriented mindset and commitment to quality and safety.

Responsibilities

• Run and support processes including bioreactor operations, clarification, chromatography, and filtration.
• Perform in-process sampling and conduct basic analytical testing as required.
• Maintain accurate electronic batch records and document activities in compliance with cGMP.
• Collaborate with cross-functional teams to support safety, product quality, and on-time delivery.
• Support investigations and contribute to continuous improvement efforts.
• Develop exposure to advanced technologies and work on global biopharma initiatives.

Skills

cGMP knowledge

Bioprocess unit operations

Sampling & analytical testing

Attention to detail

Team collaboration

Job description

Manufacturing Biotechnologist 1

Execute

• Run and support processes including bioreactor operations, clarification, chromatography, and filtration.
• Perform in-process sampling and conduct basic analytical testing as required.
• Maintain accurate electronic batch records and document activities in compliance with cGMP.
• Collaborate with cross-functional teams to support safety, product quality, and on-time delivery.
• Support investigations and contribute to continuous improvement efforts.
• Develop exposure to advanced technologies and work on global biopharma initiatives.

Manufacturing Biotechnologist 1

Execute cGMP biopharmaceutical manufacturing activities in a highly regulated environment, supporting both upstream and/or downstream operations.

Key duties

• Run and support processes including bioreactor operations, clarification, chromatography, and filtration.
• Perform in-process sampling and conduct basic analytical testing as required.
• Maintain accurate electronic batch records and document activities in compliance with cGMP.
• Collaborate with cross-functional teams to support safety, product quality, and on-time delivery.
• Support investigations and contribute to continuous improvement efforts.
• Develop exposure to advanced technologies and work on global biopharma initiatives.

Qualifications/skills

• Knowledge of cGMP manufacturing and compliance expectations.
• Hands-on experience with bioprocess unit operations (e.g., bioreactors, chromatography, filtration).
• Ability to perform routine sampling and basic analytical testing.
• Strong attention to detail for batch record accuracy and documentation.
• Team-oriented mindset and commitment to quality and safety.