Senior GMP Manufacturing Technician - 2nd Shift (Onsite)

Alnylam Pharmaceuticals; Norton (MA); Sur place; USD 83 000 - 112 000; Plein temps

Avantages offerts par ce poste

Medical, dental, and vision coverage

Life and disability insurance

401(k) with company match

Paid time off

Résumé du poste

Alnylam Pharmaceuticals is seeking a Manufacturing Operator for the Norton, MA facility to run GMP production on a second shift (Wed–Sat, 2:00 pm–12:00 am). You will operate weigh/dispense, solution prep, chemical synthesis, UF/DF, HPLC, annealing, concentration and lyophilization, while ensuring accurate documentation and safety compliance.

The ideal candidate has a BS with 5–7 years in a regulated GMP setting, strong attention to detail, and the ability to train peers across multiple

Qualifications

• BS degree preferred with 5–7 years' experience in a regulated GMP facility.
• Must possess mechanical and scientific aptitude and document work clearly.
• Strong safety, compliance, and attention to detail.
• Ability to perform strenuous physical work in cleanroom environments.

Responsabilités

• Execute cGMP manufacturing operations using SOPs and batch records with accurate documentation.
• Troubleshoot equipment issues and coordinate with support groups to minimize impact.
• Maintain safe, compliant work environment and support safety investigations and CAPAs.
• Initiate deviations and eQMS records with QA and leadership.
• Lead and mentor peers across multiple manufacturing areas and support NPI/tech transfers.

Connaissances

Mechanical aptitude

Scientific aptitude

Team leadership

English communication

Time management

Safety compliance

Documentation

Problem solving

Formation

Bachelor of Science (BS) degree

Outils

Unicorn

MS Word

Excel

Description du poste

Alnylam Pharmaceuticals is seeking a Manufacturing Operator for the Norton, MA facility to run GMP production on a second shift (Wed–Sat, 2:00 pm–12:00 am). You will operate weigh/dispense, solution prep, chemical synthesis, UF/DF, HPLC, annealing, concentration and lyophilization, while ensuring accurate documentation and safety compliance.

The ideal candidate has a BS with 5–7 years in a regulated GMP setting, strong attention to detail, and the ability to train peers across multiple