Drug Product Senior Specialist, Nantong-QA (Nantong, JS, CN, 226000)
About this opportunity
About the role:
As a Drug Product Senior Specialist in Nantong QA, you’ll oversee on-site quality for drug product manufacturing. You’ll help ensure production activities meet GMP requirements and company quality standards, supporting compliant operations and product release.
Working with Production, QC and Engineering, you’ll oversee manufacturing activities, review batch records and quality documents, and support investigations, audits and inspections. Your work will help teams identify quality risks and address them in a timely manner.
Your contribution:
Oversee drug product manufacturing activities, including solution preparation, filtration, filling, packaging, cleaning and disinfection, and line clearance, to ensure compliance with GMP and company quality standards
Review batch production records and related documents for completeness, accuracy and compliance
Participate in investigations and resolution of deviations, change controls and corrective and preventive actions
Review and improve production procedures, batch records and other quality documents
Support product release by ensuring required documentation reviews are complete
Participate in internal and customer audits and regulatory inspections, and help implement corrective actions
A good match:
Bachelor’s degree or higher in bioengineering, biotechnology, pharmacy, chemistry or a related field
Experience in pharmaceutical manufacturing quality management, ideally with on-site QA experience in drug product production
Knowledge of China GMP regulations, pharmaceutical quality management systems and drug product manufacturing processes
Familiarity with deviation investigations, change controls, corrective and preventive actions, and batch record review
Experience in on-site QA for aseptic processing, fill-finish or biologics manufacturing is an advantage
Strong communication and problem-analysis skills, a responsible and detail-oriented approach, and CET-4 English proficiency or above, with the ability to read English quality and technical documents
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 266 comparable Senior Quality roles across 63 biopharma companies.
Salary context
66 of 266 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 266 comparable roles
+ 28 more countries
Seniority mix
266 of 266 peers have a known seniority level
Therapeutic area mix
0 of 266 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
Notify me about similar jobs
Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
Or follow a whole field: get every new Quality job in China, and choose locations and companies.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.