QC SAMPLE COORDINATOR l
Company: PCI Pharma Services
Location: Bedford
Posted on: April 1, 2026
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Job Description:
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. JOB DESCRIPTION:
Position Title : QC Sample Coordinator I Location: Bedford, New
Hampshire Department: Quality Control / Incoming materials
Reporting To: QC Supervisor, Sample Management Responsible For
(Staff): No This position will have responsibility for supporting
activities in the QC Sample Management group, which includes use of
material control procedures and specification documents, raw
material sampling & inspection, participation in the coordination
of testing with internal and external resources, and collection of
data and material certificates for review by QA. ESSENTIAL DUTIES
AND RESPONSIBILITIES: Ordering, receipt and management of QC
Laboratory supplies, including chemicals, reference standards, and
consumable materials in accordance with cGMP and procedural
requirements Inspection, review and receipt of incoming samples for
testing. Verification of information against specifications,
protocols, and other documentation to ensure compliance. Maintain
sample tracking and chain of custody records in accordance with
cGMP and procedural requirements Complete data entry in validated
systems and business tools with a high degree of accuracy. Request,
assemble, and distribute QC testing data packets for support of
in-process, lot release, raw material, and stability testing Assist
with coordinating external testing Request and maintain Quality
Control logbooks in accordance with cGMP and procedural
requirements Perform inspections on packaging components
QUALIFICATIONS: Required: 1-3 years relevant business experience
Proficient in MS Office. Must have strong attention to detail as
well as ability to work in a cross-functional team environment
Professional interpersonal skills and the ability to communicate
well orally and in writing Ability to multi-task in a dynamic
environment with changing priorities Preferred: ? Ability to work
independently as well as on a team, with limited supervisory
oversight Master Control experience a plus cGMP experience a plus
LI-RS1 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.
Keywords: PCI Pharma Services, Lawrence , QC SAMPLE COORDINATOR l, Science, Research & Development , Bedford, Massachusetts
