Confidential
Job Title:
Quality Control (QC) Chemist II – Method Validation
Industry:
Pharmaceutical Manufacturing Location:
Fall River, MA Job Type:
Full-Time | On-site Work Hours:
8:30 AM – 5:00 PM (may vary based on business needs) Reports To:
QC Manager
Required Citizenship / Work Permit / Visa Status: ~ US Citizen/Green Card Holder/TN Visa/H1B Transfers/OPT-EAD
About the Role We are seeking an experienced
Quality Control (QC) Chemist II
to join our QC team in Fall River, MA. The QC Chemist will perform testing of samples using advanced analytical methods and specialized laboratory instruments to ensure compliance with cGMP, data integrity, and regulatory guidelines. This role focuses heavily on
method validation, method verification, and method transfer
within a fast-paced pharmaceutical environment.
Key Responsibilities Prepare and execute analytical
method validation, verification, and transfer protocols
. Perform
cleaning validation (residue analysis) and raw material testing/release. Conduct advanced and routine laboratory testing using instruments such as
HPLC, GC, ICP, Karl Fischer, Particle Size Analyzer
, and more. Ensure strict adherence to
cGMP, GLP, and good documentation practices
. Lead investigation activities and participate in compliance audits as required. Maintain accurate lab records and support continuous improvement initiatives. Collaborate with cross-functional teams to ensure project deadlines and quality standards are met.
Education & Experience Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or related physical sciences required. Minimum 2 years of recent QC Chemist experience
in a
pharmaceutical company
(generic pharma preferred). Strong hands-on expertise with
analytical method validation, verification, and transfer
. Must have
small molecule experience
. Proficiency in
cGMP, SOP compliance, and data integrity
. Experience with inhalation products (MDI) is a strong plus. Excellent English communication skills (reading, writing, and technical discussions).
Working Conditions On-site role in a
cGMP laboratory
. Requires use of PPE (lab coat, safety glasses, gloves, etc.). May involve working with solvents, powders, or pharmaceutical raw materials. Some evening, weekend, or holiday work may be required. No remote work available.
Physical Requirements Standing/walking unassisted for up to 75% of an 8-hour shift. Lifting up to 10 kg when required. Ability to work at a computer or laboratory bench for extended periods.
Quality Control (QC) Chemist II – Method Validation
Industry:
Pharmaceutical Manufacturing Location:
Fall River, MA Job Type:
Full-Time | On-site Work Hours:
8:30 AM – 5:00 PM (may vary based on business needs) Reports To:
QC Manager
Required Citizenship / Work Permit / Visa Status: ~ US Citizen/Green Card Holder/TN Visa/H1B Transfers/OPT-EAD
About the Role We are seeking an experienced
Quality Control (QC) Chemist II
to join our QC team in Fall River, MA. The QC Chemist will perform testing of samples using advanced analytical methods and specialized laboratory instruments to ensure compliance with cGMP, data integrity, and regulatory guidelines. This role focuses heavily on
method validation, method verification, and method transfer
within a fast-paced pharmaceutical environment.
Key Responsibilities Prepare and execute analytical
method validation, verification, and transfer protocols
. Perform
cleaning validation (residue analysis) and raw material testing/release. Conduct advanced and routine laboratory testing using instruments such as
HPLC, GC, ICP, Karl Fischer, Particle Size Analyzer
, and more. Ensure strict adherence to
cGMP, GLP, and good documentation practices
. Lead investigation activities and participate in compliance audits as required. Maintain accurate lab records and support continuous improvement initiatives. Collaborate with cross-functional teams to ensure project deadlines and quality standards are met.
Education & Experience Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Chemistry, or related physical sciences required. Minimum 2 years of recent QC Chemist experience
in a
pharmaceutical company
(generic pharma preferred). Strong hands-on expertise with
analytical method validation, verification, and transfer
. Must have
small molecule experience
. Proficiency in
cGMP, SOP compliance, and data integrity
. Experience with inhalation products (MDI) is a strong plus. Excellent English communication skills (reading, writing, and technical discussions).
Working Conditions On-site role in a
cGMP laboratory
. Requires use of PPE (lab coat, safety glasses, gloves, etc.). May involve working with solvents, powders, or pharmaceutical raw materials. Some evening, weekend, or holiday work may be required. No remote work available.
Physical Requirements Standing/walking unassisted for up to 75% of an 8-hour shift. Lifting up to 10 kg when required. Ability to work at a computer or laboratory bench for extended periods.