Senior Logistics Specialist

TekWissen LLC; Portsmouth (NH); On-site; USD 27,552 - 34,440; Full time

Job summary

A global workforce management provider is seeking someone to dispense raw materials under cGMP standards in a biomanufacturing environment. Responsibilities include executing dispensing processes, monitoring equipment, and ensuring compliance with safety regulations. Prior experience in pharmaceutical settings and familiarity with dispensing software are essential. Strong attention to detail and documentation skills are required. Join a team committed to delivering innovative medicines in Portsmouth, New Hampshire.

Qualifications

• Experience in a biomanufacturing environment with adherence to cGMP standards.
• Ability to handle pharmaceuticals safely and effectively.
• Attention to detail in documentation and procedures.

Responsibilities

• Dispense raw materials and maintain compliance with cGMP standards.
• Execute dispensing processes and basic lab tasks.
• Monitor equipment and ensure training records are current.
• Conduct peer reviews of completed orders after training.
• Participate in safety inspections and promote safe practices.

Skills

Prior experience in pharmaceutical or biomanufacturing environments

Familiarity with material handling systems

Understanding of basic lab instrumentation

Basic understanding of cGMP compliance

Good communication skills

Tools

eDispense

Job description

Shift: Day Shift - 07:00 AM to 07:00 PM - Rotating Days, and every other weekend

Pay Rate: $20.00-$25.00/hr

Overview

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide. Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.

Summary

Responsible for dispensing raw materials, liquids, powders (hazardous and non-hazardous), and acids/bases, under cGMP conditions to support the manufacture of therapeutic proteins (API). The role involves executing dispensing processes, ensuring compliance with cGMP and GDP standards, maintaining documentation, and adhering to all safety and procedural requirements.

Responsibilities

• Perform and monitor all dispensing processes and weighing activities for liquids, powders, acids, and bases.
• Follow and adhere to written procedures (SOPs) while working in a Class C environment with appropriate PPE.
• Execute process recipes and maintain compliance with cGMP and GDP documentation standards.
• Monitor equipment and processes; perform basic lab tasks such as pH measurement, conductivity, and sampling.
• Maintain qualification for assigned tasks and ensure training records are current.
• Perform cleaning and sanitization of dispensing equipment per schedule.
• Conduct peer and first-level reviews of completed eDispense orders/kits after appropriate training signoffs.
• Prepare materials for transport and delivery to manufacturing suites and record material movements in software systems.
• Participate in safety inspections and report safety observations to promote a safe work environment.
• Attend shift exchanges, meetings, and complete administrative tasks such as email communication and project participation.
• Perform other duties as assigned to support the Logistics Team.

Required Skills

• Prior experience in pharmaceutical or biomanufacturing environments.
• Familiarity with material handling systems, dispensing software (e.g., eDispense), and electronic batch record systems.
• Understanding of basic lab instrumentation (pH meters, conductivity meters).
• Participation in safety programs or previous involvement in continuous improvement initiatives.
• Basic understanding of cGMP compliance and good documentation practices (GDPs).
• Demonstrated knowledge of aseptic techniques and cross-contamination prevention.
• Ability to follow SOPs and execute tasks accurately in a regulated environment.
• Proficiency in record keeping (both written and electronic).
• Strong attention to detail and adherence to safety and quality procedures.
• Capability to perform routine equipment cleaning, sanitization, and documentation reviews.
• Good communication skills and ability to work effectively within a team environment.

TekWissen® Group is an equal opportunity employer supporting workforce diversity.