QC Specialist II, Analytical Investigations
PCI Pharma Services · Bedford, NH
- Level
- Specialist
- Team
- Quality
- Degree
- Preferred
- Experience asked
- 5+ years
- Industry
- Pharma & life sciences
- Posted
- 30+ days ago
The role in 30 seconds
A specialist quality role at PCI Pharma Services (pharma & life sciences) in Bedford, NH. You will.
- They ask for
- 5+ years · degree preferred
- Tools it names
- FDA / GMP, Validation (IQ/OQ/PQ)
Read from the posting. The full description is below.
How this role compares
Against 37 other live quality postings in New Hampshire.
- Base pay
- Not listed in this posting
- Experience asked
- Typical (5+ years)
Typical $97k–$165k, from 15 postings that list pay.
Similar roles usually ask 5+ years.
Skills these teams ask for most
- Root cause 71%
- Lean 47%
- Six Sigma 45%
- Supplier quality 42%
- AS9100 39%
- ✓ FDA / GMP 37%
✓ = this posting asks for it too. % = share of similar postings that mention it.
At a glance
Pulled from the posting text. If it's not listed here, the posting didn't say.
How to get in at this plant
Five moves over a week or two. The first one takes ten minutes.
- 1
Pick 2–3 people on the Quality team at PCI Pharma Services
We found 2 people at this company and state: 2 on the team. Engineers who joined in the last year or two reply the most. See them ↓
- 2
Send a short, curious note
One real question about their work. No favors yet. Each person gets a different note, written for this role.
Write to Jill → (free) - 3
Turn a reply into a short call
Questions worth asking about this team:
- What does a normal week look like on your team?
- Which standards drive the work here: ISO 13485, IATF 16949, AS9100?
- How much of the job is customer complaints versus prevention?
- How did you land the job? What stood out in your interviews?
- 4
Apply with someone vouching for you
If the call went well, ask whether they’d pass your résumé to the hiring manager. Send your résumé link, apply that day, and let them know.
- 5
Bring proof to the interview
One page of before-and-after numbers from projects you led: scrap, OEE, cycle time, cost. Plant managers hire on results.
This plant: PCI Pharma Services in Bedford
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Full description from PCI Pharma ServicesAs posted on their careers site.ShowHide
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.
What You’ll Do
As a QC Specialist, you will
- •Lead investigations into QC Analytical deviations, OOS/OOT/OOE results, and other quality issues.
- •Serve as a key point of contact during audits and inspections, ensuring timely and compliant responses.
- •Draft and revise change controls, technical reports, cGMP documents, and protocols.
- •Perform QC analytical testing, review data, and identify trends to proactively address risks.
- •Assist in managing analytical equipment to maintain compliance and efficiency.
- •Collaborate cross-functionally to close out quality events and audit findings on time.
- •Help shape and refine QC processes that support continuous improvement.
Show full description ↓Show less ↑
What You Bring
- •Education/Experience: Bachelor’s degree in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or related field; 2–5 years of QC Analytical Chemistry experience (pharma experience preferred).
- •Technical Skills: Hands-on experience with UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer, and Osmometer.
- •Knowledge: Solid understanding of cGMP, ICH, USP, and global compendia guidelines, especially in analytical method validation and stability studies.
- •Strengths: Strong organizational and documentation skills, technical writing ability, and excellent communication skills (written and verbal).
- •Mindset: Ability to thrive in a fast-paced, dynamic environment, juggling multiple priorities while maintaining a sharp eye for detail.
- •Tech: Proficiency in MS Office; experience with lab-based data management systems a plus.
Why Join Us
- •Be part of a collaborative team where your expertise directly impacts patient safety and product quality.
- •Gain exposure to diverse analytical techniques and regulatory processes.
- •Opportunity to work in a GMP environment supporting both clinical and commercial product lifecycles.
- •Professional growth through hands-on problem solving, cross-functional collaboration, and continuous learning.
Join us and be part of building the bridge between life changing therapies and patients. Let’s talk future