Manufacturing Biotechnologist 1 - Day Shift

Tailored Management; Portsmouth (NH); On-site; USD 32,000 - 43,000; Full time

Benefits offered by this job

Benefits

Job summary

The Manufacturing Biotechnologist 1 role at Tailored Management in Portsmouth, NH is a 6-month contract for day shift. You will manufacture therapeutic proteins under cGMP, perform SOPs, monitor equipment, and conduct basic lab tasks.

The schedule is a 12-hour day shift on a rotating pattern, with overnight hours on alternating weeks. Competitive pay at $26.85 per hour plus benefits; onsite work at 101 International Drive, Portsmouth.

Qualifications

• Proven logic and decision making abilities.
• Strong written and verbal communication skills are required.

Responsibilities

• Set up, operate equipment, and monitor production processes, including CIP/SIP operations and report production in documents per GMP/GDP.
• Attain qualification for all assigned tasks and maintain individual training plan.
• Perform basic laboratory tasks, such as pH, conductivity, test product samples, etc.
• Perform material movements, transfer raw materials and chemicals into/out of production areas.
• Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.
• Administrative tasks – attending shift exchanges, meetings, emails, and project participation.
• Perform other duties as assigned.

Skills

Logic & decision making

Written & verbal communication

Job description

Title

Manufacturing Biotechnologist 1 - Day Shift

Job ID

#26-02743

Pay

Up to $26.85 per hour Portsmouth, NH Onsite

Location

101 International Drive, Portsmouth, NH

Contract

6 Months - possibility for extension or FTE conversion

Pay Rate

$26.85 per hour + Benefits

Shift

Day Shift (6:00 AM - 6:30 PM)

Shift Details

This is a 12-hour Day Shift (6:00 AM - 6:30 PM) on a rotating schedule. Employees work Monday, Tuesday, Friday, Saturday, and Sunday one week, followed by Wednesday and Thursday the next week. Candidates must be comfortable with this alternating schedule and overnight hours.

Job Description

The Manufacturing Associate Level I is responsible for the manufacture of therapeutic proteins (API) under cGMP conditions. Level I 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.

Roles and Responsibilities

• Set up, operate equipment, and monitor production processes, including clean-in-place (CIP) and steam-in-place (SIP) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation procedures (GDPs), review documentation as appropriate.
• Attain qualification for all assigned tasks and maintain individual training plan.
• Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
• Perform material movements, transfer raw materials, chemicals into, out of,across the production areas.
• Maintain facility and equipment through routine cleaning and sanitization, support 6S programs.
• Administrative tasks – attending shift exchange, meetings, sending/receiving emails, participating in projects.
• Perform other duties as assigned.

Skills

• Proven logic and decision making abilities, critical thinking skills
• Strong written and verbal communication skills are required