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Formulation Technician

Job in Bedford, Hillsborough County, New Hampshire, 03110, USA
Listing for: PCI Pharma Services
Full Time position
Listed on 2026-01-12
Job specializations:
  • Manufacturing / Production
    Quality Engineering, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 60000 USD Yearly USD 60000.00 YEAR
Job Description & How to Apply Below
Position: Formulation Technician I

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

This position will have the primary responsibility for daily formulation activities to ensure schedule activities are completed, formulation materials and equipment are maintained, as well as the responsibility for performing corrective and preventative actions. As a secondary function, provide troubleshooting expertise for manufacturing of products both internally and externally of the company.

Essential Duties and Responsibilities

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The basic duties and responsibilities include the following, but other duties may be assigned.

  • Has ownership for the daily formulation activities to ensure scheduled all scheduled tasks/events are completed

  • Is responsible for critical steps in the formulation process including but not limited to, lab setup and process flows, in-process testing, API dissolution and final QS while ensuring safety, batch integrity and prevention or errors that could lead to product and or finical loss

  • Initiate the production of batch documentation used for engineering and cGMP production.

  • Prepare and update Master Production Batch records and SOPs accurately for communicating and initiate the documentation change process for needed documentation changes

  • Complete executed Batch Records accurately and completely prior to submission to supervision for review

  • Comply with all area SOPs and ensure logbooks are completed, and adhere to cGMP requirements

  • Author process deviations when these occur within the department, participate in investigations, and contribute to identifying corrective and preventative actions

  • Cross train to increase technical skills across the department

  • Accountable for timely communication to management and clients of issues, challenges as well as opportunities for process improvements.

  • As a member of the manufacturing team, you will perform other manufacturing tasks for example filling, capping etc., as needed.

  • Work with enabling groups to improve/implement processes.

  • Other duties as assigned.

  • Strong interpersonal skills

  • Strong working knowledge of MS Office suite is preferable

  • Attention to detail and positive attitude are key attributes

  • Able to follow rules and regulations perfectly

  • Works directly with aseptic and non-aseptic personnel. Works closely with Quality Assurance, MTS, Validation etc.

Qualifications

The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Required
  • High School education or AS degree or BS degree in Chemical Engineering/ Bio Chemistry or other industry related discipline is preferred

  • Experience and knowledge of formulation/compounding tools and equipment

  • Minimum 1-2 year’s work experience in a GMP environment preferably in fill finish pharmaceutical operations

  • Demonstrated ability to prioritize multiple projects and activities Full Professional Proficiency:
    Ability to speak, read, and write fluently and accurately on all levels pertinent to professional needs.

#LI-KC1

Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose:
Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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