8:30 AM - 5:00 PM (may vary based on business needs)
About the Role
We are seeking an experienced
Quality Control Chemist II
to join our growing pharmaceutical manufacturing team. This position is responsible for performing analytical testing of Metered Dose Inhaler (MDI) products and related materials in compliance with cGMP and regulatory standards. The ideal candidate will bring strong analytical experience, attention to detail, and a commitment to quality in a regulated environment.
Key Responsibilities
Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, and other analytical instruments.
Conduct method validation, transfer, and verification studies as per approved protocols.
Review and interpret analytical data to ensure compliance with specifications.
Document all results accurately in laboratory notebooks and LIMS per cGMP requirements.
Participate in OOS/OOT investigations and support CAPA implementation.
Ensure instruments are calibrated, qualified, and maintained as per schedule.
Comply with all safety, quality, and regulatory procedures.
Support continuous improvement in laboratory practices and documentation.
Qualifications
Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or related field.
3-6 years of relevant QC laboratory experience in a cGMP-regulated pharmaceutical environment.
Hands-on experience with
HPLC, GC, UV, FTIR
, and wet chemistry techniques.
Experience working with
MDI/DPI or inhalation products
preferred.
Strong understanding of
FDA, ICH, and cGMP
regulations.
Excellent documentation, analytical, and communication skills.
Work Schedule
Full-time | Onsite | 1st Shift
Monday to Friday
Compensation
Compensation is based on experience and qualifications.
Candidates are encouraged to share their
expected hourly rate or base salary range
when applying.
Benefits
Health, Dental & Vision Insurance
Paid Time Off & Holidays
401(k) Retirement Plan
Career growth and professional development opportunities
Job Type: Full-time
Benefits:
401(k)
Dental insurance
Health insurance
Health savings account
Life insurance
Paid time off
Professional development assistance
Relocation assistance
Retirement plan
Vision insurance
Application Question(s):
How many years of Quality Control (QC) experience do you have in the pharmaceutical industry?
What analytical instruments are you proficient with (e.g., HPLC, GC, UV, FTIR)?
How many years of experience with cGMP or FDA-regulated manufacturing environments do you have?
What is your expected hourly rate or base salary for this position?
What is your work authorization/ Work Permit / Visa Status in the USA?
Please share your regular email and regular phone number.
Are you based nearby Fall River, MA; or are you willing to relocate to Fall River, MA for this position? Please share your location. (City, State & Zip code)
What are the best hours or times to call you?
Education:
Bachelor's (Required)
Work Location: On the road
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