What are the responsibilities and job description for the Quality Assurance Specialist position at Akkodis?
Job Description:
Akkodis is seeking a Validation Specialist for a Contract job. As a key member of the team, you will support Adjuvant manufacturing activities related to engineering, investigational, definition, development and process validation runs.
The ideal candidate will have experience in biological processes or analytics in a cGMP environment and possess strong analytical skills. You will be responsible for writing protocols, reports, procedures and memos as needed to support manufacturing activities.
This is an excellent opportunity to work with a dynamic team and contribute to the success of Akkodis. If you are a motivated and detail-oriented individual with a passion for quality assurance, we encourage you to apply.
Key Responsibilities:
• Support execution and documentation of engineering, development and/or validation studies
• Lead or supervise groups and task forces in the planning of engineering, investigational, definition, development and process validation runs
• Input to design space / DOE studies through establishment of scale-up / scale-down parameters utilizing engineering fundamentals
Requirements:
• BS or MS in basic sciences, math, engineering or pharmacy
• 2 years' experience in biological processes or analytics in a cGMP environment
• Strong analytical skills and attention to detail
• Ability to work in a fast-paced environment and prioritize tasks effectively
Benefits:
Akkodis offers a comprehensive benefits package, including medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Akkodis is seeking a Validation Specialist for a Contract job. As a key member of the team, you will support Adjuvant manufacturing activities related to engineering, investigational, definition, development and process validation runs.
The ideal candidate will have experience in biological processes or analytics in a cGMP environment and possess strong analytical skills. You will be responsible for writing protocols, reports, procedures and memos as needed to support manufacturing activities.
This is an excellent opportunity to work with a dynamic team and contribute to the success of Akkodis. If you are a motivated and detail-oriented individual with a passion for quality assurance, we encourage you to apply.
Key Responsibilities:
• Support execution and documentation of engineering, development and/or validation studies
• Lead or supervise groups and task forces in the planning of engineering, investigational, definition, development and process validation runs
• Input to design space / DOE studies through establishment of scale-up / scale-down parameters utilizing engineering fundamentals
Requirements:
• BS or MS in basic sciences, math, engineering or pharmacy
• 2 years' experience in biological processes or analytics in a cGMP environment
• Strong analytical skills and attention to detail
• Ability to work in a fast-paced environment and prioritize tasks effectively
Benefits:
Akkodis offers a comprehensive benefits package, including medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, an EAP program, commuter benefits, and a 401K plan. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
