Operate production equipment according to Standard Operating Procedures (SOPs), Batch Records, Manufacturing Directions (MD), and Manufacturing Operating Procedures (OPM). Execute all procedures associated with cross-linked hyaluronic acid product production, review manufacturing documentation for compliance, coordinate sample preparation and testing, record data into Batch Records, log books, and OPMs, document all work activities according to Good Documentation Practices, and recommend document revisions. Report procedural deviations and nonconformance to management.
**Must have experience with GMP**
ResponsibilitiesOperate production equipment according to SOPs, Batch Records, MD, and OPM.Execute procedures associated with cross-linked hyaluronic acid product production.Review manufacturing documentation for compliance.Coordinate sample preparation and testing.Record data into Batch Records, log books, and OPMs.Document all work activities according to Good Documentation Practices and recommend document revisions.Report procedural deviations and nonconformance to management.Essential SkillsExperience with SOPs, GMP, and Batch Records.Experience in pharmaceutical manufacturing.Knowledge of cell culture, chemicals (acids and bases), and aseptic techniques.Experience with SAP.Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing environments.Additional Skills & QualificationsAssociate or bachelor's degree with 1-4 years of biomanufacturing/pharmaceutical experience.Strong attention to detail and initiative.Team-oriented and hardworking.Work Environment
The work shift is from 6:00 AM to 2:30 PM, with potential changes to 10-hour days over 4 days a week. You will work on the first shift with 6-8 team members in a business casual environment. The company values hardworking, detail-oriented, and team-oriented individuals who take initiative.
If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com.
Pay and BenefitsThe pay range for this position is $20.00 - $25.00
• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in Bedford,MA.
Application Deadline
This position will be accepting applications until Dec 20, 2024.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.