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Quality Control Chemistry Project Management

  • Quality Control Chemistry Project Management job type Posted on: Nov 03, 2026
  • Quality Control Chemistry Project Management experience level Stark Pharma Solutions Inc
  • Quality Control Chemistry Project Management employment type New Haven, Connecticut
  • Quality Control Chemistry Project Management employment type Onsite
  • Quality Control Chemistry Project Management salary Full-time

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Job Title :

Quality Control Chemistry Project Management

Job Type :

Full-Time

Job Location :

New Haven Connecticut United States

Remote :

No

Jobcon Logo Job Description :

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT.

Position: Quality Control Chemistry & Project Management
Location: Connecticut
Duration: Long Term

Job Overview

We are seeking QC professionals with 3 6 years of experience for Chemistry-focused and Project Management-focused roles in the pharmaceutical industry. Candidates should have relevant experience in quality control, laboratory operations, documentation, or project coordination, depending on the position.

Key Responsibilities

  • Perform QC testing, review results, and maintain accurate laboratory records (Chemistry roles).
  • Support analytical testing, data review, and investigation of out-of-specification (OOS) results.
  • Ensure compliance with GMP, SOPs, and quality standards.
  • Support QC projects, timelines, deliverables, and project documentation (PM-focused roles).
  • Coordinate with QC, QA, laboratory, and cross-functional teams.
  • Track project progress, identify issues, and support timely resolution.
  • Maintain accurate reports, records, and quality documentation.

Required Qualifications

  • 3 6 years of relevant experience in QC Chemistry or QC Project Management.
  • Experience in the pharmaceutical or regulated industry.
  • Knowledge of GMP, SOPs, and quality documentation.
  • Chemistry roles: Experience with analytical testing techniques such as HPLC, GC, UV, or other relevant instruments.
  • PM-focused roles: Experience in project coordination, timeline tracking, reporting, and stakeholder communication.
  • Strong analytical, organizational, and problem-solving skills.
  • Good communication and teamwork skills.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.

Jobcon Logo Position Details

Posted:

Nov 03, 2026

Reference Number:

2573-34797

Employment:

Full-time

City:

New Haven

Job Origin:

CIEPAL_ORGANIC_FEED

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About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT.

Position: Quality Control Chemistry & Project Management
Location: Connecticut
Duration: Long Term

Job Overview

We are seeking QC professionals with 3 6 years of experience for Chemistry-focused and Project Management-focused roles in the pharmaceutical industry. Candidates should have relevant experience in quality control, laboratory operations, documentation, or project coordination, depending on the position.

Key Responsibilities

  • Perform QC testing, review results, and maintain accurate laboratory records (Chemistry roles).
  • Support analytical testing, data review, and investigation of out-of-specification (OOS) results.
  • Ensure compliance with GMP, SOPs, and quality standards.
  • Support QC projects, timelines, deliverables, and project documentation (PM-focused roles).
  • Coordinate with QC, QA, laboratory, and cross-functional teams.
  • Track project progress, identify issues, and support timely resolution.
  • Maintain accurate reports, records, and quality documentation.

Required Qualifications

  • 3 6 years of relevant experience in QC Chemistry or QC Project Management.
  • Experience in the pharmaceutical or regulated industry.
  • Knowledge of GMP, SOPs, and quality documentation.
  • Chemistry roles: Experience with analytical testing techniques such as HPLC, GC, UV, or other relevant instruments.
  • PM-focused roles: Experience in project coordination, timeline tracking, reporting, and stakeholder communication.
  • Strong analytical, organizational, and problem-solving skills.
  • Good communication and teamwork skills.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.

Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse backgrounds.

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