Manufacturing Associate II
Biogen
6 months ago
On-site
Triangle, NC
Operations
Schedule/Operations:
- 12-hour shifts (Nights 6p–6a) on a 2-2-3 calendar rotation; facilities operate 24/7
Role (Drug Substance facility – Research Triangle Park, RTP):
- Downstream/Purification manufacturing in a cGMP-governed environment.
- Downstream/Purification steps: Column Chromatography; Viral Filtration; Ultra-Filtration; Bulk Dispensing of the drug substance.
What You’ll Do:
- Execute daily manufacturing activities, including operating process equipment and executing validation protocols per cGMP SOPs.
- Document and record all cGMP data/information (including deviations) for processing steps and equipment activities; create/revise batch records, SLRs, and equipment logbooks.
- Assist with in-process sampling and sampling analysis (e.g., pH, conductivity, protein concentration, osmolarity, cell counts).
- Maintain a clean and safe work environment with a focus on audit readiness of process areas.
- Be a team player and leader; contribute consistently.
- Participate in and lead training and development initiatives for personal growth and team development.
Requirements:
- Bachelor’s Degree (STEM preferred), OR
- BioWork Certificate or Associate’s Degree with transferrable experience, OR
- High School Diploma (or equivalent) plus at least 6 months of direct and/or military experience.
Benefits (as listed):
- Medical, Dental, Vision, & Life insurances; fitness & wellness programs (fitness reimbursement); Short- and Long-Term Disability; paid vacation (minimum 15 days) plus end-of-year shutdown (Dec 26–Dec 31); up to 12 paid holidays + 3 personal significance days; sick time (80 hours/year); Paid Maternity and Parental Leave; 401(k) with company match; Employee stock purchase plan; tuition reimbursement up to $10,000/year; Employee Resource Groups participation.
Compensation (as stated):
- Base compensation range: $23.56–$30.77.
- 12-hour shifts (Nights 6p–6a) on a 2-2-3 calendar rotation; facilities operate 24/7
Role (Drug Substance facility – Research Triangle Park, RTP):
- Downstream/Purification manufacturing in a cGMP-governed environment.
- Downstream/Purification steps: Column Chromatography; Viral Filtration; Ultra-Filtration; Bulk Dispensing of the drug substance.
What You’ll Do:
- Execute daily manufacturing activities, including operating process equipment and executing validation protocols per cGMP SOPs.
- Document and record all cGMP data/information (including deviations) for processing steps and equipment activities; create/revise batch records, SLRs, and equipment logbooks.
- Assist with in-process sampling and sampling analysis (e.g., pH, conductivity, protein concentration, osmolarity, cell counts).
- Maintain a clean and safe work environment with a focus on audit readiness of process areas.
- Be a team player and leader; contribute consistently.
- Participate in and lead training and development initiatives for personal growth and team development.
Requirements:
- Bachelor’s Degree (STEM preferred), OR
- BioWork Certificate or Associate’s Degree with transferrable experience, OR
- High School Diploma (or equivalent) plus at least 6 months of direct and/or military experience.
Benefits (as listed):
- Medical, Dental, Vision, & Life insurances; fitness & wellness programs (fitness reimbursement); Short- and Long-Term Disability; paid vacation (minimum 15 days) plus end-of-year shutdown (Dec 26–Dec 31); up to 12 paid holidays + 3 personal significance days; sick time (80 hours/year); Paid Maternity and Parental Leave; 401(k) with company match; Employee stock purchase plan; tuition reimbursement up to $10,000/year; Employee Resource Groups participation.
Compensation (as stated):
- Base compensation range: $23.56–$30.77.