Bioprocess Lead — Night Shift (6pm–6am)

Biopharma Careers; Sanford (NC); Hybrid; USD 60,000 - 100,000; Full time

Benefits offered by this job

401(k) with Pfizer matching

Pfizer Retirement Savings Contribution

Paid vacation

Holiday and personal days

Medical, dental and vision benefits

Job summary

Pfizer is seeking a Senior Bioprocess Technician for a 12-hour night shift (6pm-6am) in Sanford, NC. The role requires 6+ years in biopharmaceutical manufacturing and hands-on experience with unit operations and automation systems.

The position offers a competitive hourly rate $28.76–$47.93, with overtime eligibility and comprehensive benefits. You will lead, train, and support team members while ensuring compliance with SOPs, MBRs, and regulatory guidelines.

Qualifications

• Minimum 6+ years of experience in biopharmaceutical manufacturing or related operations.
• Experience with biopharmaceutical unit operations and lab operations.
• Understanding of continuous improvement processes.
• Ability to manage personal time and professional development.
• Proficient with SAP, Delta-V and other enterprise systems.

Responsibilities

• Lead and train team members in area of expertise.
• Identify and resolve potential problems proactively.
• Complete assignments independently and ensure team tasks finish.
• Review non-standard work for technical soundness.
• Adhere to Pfizer standards and guidelines.

Skills

Strong problem-solving skills

Strong communication and interpersonal

Adaptability under pressure

Education

High School Diploma or GED

Bachelor's Degree

Tools

SAP

Delta-V

Job description

Pfizer is seeking a Senior Bioprocess Technician for a 12-hour night shift (6pm-6am) in Sanford, NC. The role requires 6+ years in biopharmaceutical manufacturing and hands-on experience with unit operations and automation systems.

The position offers a competitive hourly rate $28.76–$47.93, with overtime eligibility and comprehensive benefits. You will lead, train, and support team members while ensuring compliance with SOPs, MBRs, and regulatory guidelines.