What are the responsibilities and job description for the Manufacturing Operator position at Staffing Resource Group, Inc?
Job Description
Manufacturing Operator - Scientific Career Entry Level
Location: Portsmouth, NH
Industry: Pharmaceutical
Shifts Available: Night shift (7 PM - 7 AM, 12-hour shifts, rotating schedule including weekends)
Salary: $27.00 hourly, paid weekly (Benefits Available)
Employment Type: 1-year contract, with potential for extension
Kickstart Your Scientific Career as a Manufacturing Operator!
Are you a recent graduate looking to launch your career in the scientific or pharmaceutical industry? This entry-level Manufacturing Operator role provides hands-on experience in the production of therapeutic proteins under Current Good Manufacturing Practices (cGMP). Join a team committed to advancing healthcare in a globally recognized company, developing skills in scientific manufacturing and laboratory operations.
Why This Opportunity?
The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials
Responsibilities
As a Manufacturing Operator, you'll engage in critical tasks to support the production of therapeutic proteins. Training will cover areas such as:
As a leader in staffing solutions, SRG specializes in placing professionals in industries such as pharmaceutical, biotech, and medical device. We connect talented individuals with opportunities that align with their skills and career goals, backed by a proprietary database and innovative recruitment strategies.
EOE/ADA
IND123
Manufacturing Operator - Scientific Career Entry Level
Location: Portsmouth, NH
Industry: Pharmaceutical
Shifts Available: Night shift (7 PM - 7 AM, 12-hour shifts, rotating schedule including weekends)
Salary: $27.00 hourly, paid weekly (Benefits Available)
Employment Type: 1-year contract, with potential for extension
Kickstart Your Scientific Career as a Manufacturing Operator!
Are you a recent graduate looking to launch your career in the scientific or pharmaceutical industry? This entry-level Manufacturing Operator role provides hands-on experience in the production of therapeutic proteins under Current Good Manufacturing Practices (cGMP). Join a team committed to advancing healthcare in a globally recognized company, developing skills in scientific manufacturing and laboratory operations.
Why This Opportunity?
- Gain real-world lab experience working with advanced pharmaceutical processes.
- Develop core industry skills in a dynamic environment with ongoing training and mentorship.
- Contribute to meaningful work that supports healthcare advancements worldwide.
The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow written procedures (SOPs), monitor equipment and processes, perform basic laboratory tasks, including pH, conductivity, sampling, and conduct routine sanitization tasks to maintain facility and equipment. They are expected to attain a basic understanding of cGMP compliance while training under close supervision, demonstrating aseptic technique in handling of products and materials
Responsibilities
As a Manufacturing Operator, you'll engage in critical tasks to support the production of therapeutic proteins. Training will cover areas such as:
- Process Operations: Execute process recipes, conduct CIP (clean-in-place) and SIP (steam-in-place) operations, and monitor equipment to ensure safety and quality standards.
- Laboratory Tasks: Monitor pH, conductivity, and perform sampling, enabling you to gain essential lab experience in line with cGMP compliance.
- Facility Upkeep: Participate in routine facility and equipment sanitization, support 6S programs, and contribute to maintaining a clean, efficient workspace.
- Documentation & Compliance: Follow Good Documentation Practices (GDP), track production in written and electronic formats, and attend shift exchanges and project meetings.
- Education: High school diploma or equivalent minimum (AS/BS in a science-related discipline preferred).
- Experience: 0-3 years of experience; a background in manufacturing or lab work is a plus but not required. Strong logic, decision-making, and critical thinking skills will help you succeed.
As a leader in staffing solutions, SRG specializes in placing professionals in industries such as pharmaceutical, biotech, and medical device. We connect talented individuals with opportunities that align with their skills and career goals, backed by a proprietary database and innovative recruitment strategies.
EOE/ADA
IND123
Salary : $27
