- Ensures that quality of the product is maintained, safety procedures, and company guidelines are followed.
- Manages utilization of equipment, facilities, and personnel to obtain maximum efficiency.
- Formulates and supervises processes, quality and production improvement methodologies.
- Maintains authority over budget and scheduling for the Manufacturing Operations Departments.
- Provides mentorship to managers of their functional area.
- Communicates progress of the department to the Executive Team.
- Identifies and evaluates fundamental issues or gaps that pose risk to the operations.
- Communicates corporate goals and objectives to the Manufacturing staff.
- Coordinates work with other departments to resolve issues across multiple departments.
- Leads adoption of lean practices and a continuous improvement mindset throughout manufacturing and in partnership with supporting organization to improve quality, delivery, cost, and productivity.
- Bachelor’s degree (B.A./B.S.) in a science or engineering discipline from a four-year college or university with 10 years of experience in a GMP facility manufacturing pharmaceuticals, preferably biologics or:
- Masters/Doctorate in a science or engineering discipline with 6-8 years of experience in a GMP facility manufacturing pharmaceuticals, preferably biologics.
- 7-15 years leading teams and managing operational budgets.
- Lean Six Sigma, Green Belt or Black Belt certification.
- You have a "bring it on!" team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.
- Your written and verbal skills are out of this world, and you communicate with clarity and confidence.
- You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.
- You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.
Skills Required
- Bachelor's degree in a science or engineering discipline and 10 years of experience in a GMP pharmaceutical manufacturing facility, preferably biologics
- Master's or doctorate in a science or engineering discipline and 6-8 years of experience in a GMP pharmaceutical manufacturing facility, preferably biologics
- 7-15 years of experience leading teams and managing operational budgets
- Lean Six Sigma Green Belt or Black Belt certification
Avid Bioservices Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Avid Bioservices and has not been reviewed or approved by Avid Bioservices.
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Healthcare Strength — Health coverage includes medical, dental, and vision alongside life and disability insurance. Plan breadth is presented as solid, with health benefits frequently highlighted as a strong element of the package.
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Equity Value & Accessibility — An Employee Stock Purchase Plan with a discounted purchase feature and the availability of stock grants provide accessible ownership opportunities. These components add long-term value beyond base pay.
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Fair & Transparent Compensation — Pay ranges are posted for some roles, offering upfront clarity on expected compensation. This transparency supports clearer expectations during hiring.
Avid Bioservices Insights
What We Do
Avid Bioservices is transforming the CDMO experience, with more than 30 years of unrivaled experience manufacturing biologics, and world-class mammalian protein facilities. We’ve produced more than 250 commercial batches, and 5 commercial products marketed in 90+ countries. For more than 10 years, we’ve maintained a flawless quality track record which we’re committed to uphold. We do it right the first time, which saves money and time. From early-stageto late-stage, concept to market, every part of our process is personalized. We’re your advocates, your trusted experts, your true partners.








