Senior Analyst, Quality Control (Raw Materials)

Ocular Therapeutix; Bedford; On-site; GBP 70,000 - 81,000; Full time

Job summary

Ocular Therapeutix, Inc. is seeking a QC Senior Analyst – Raw Materials to ensure compliance with cGMP and regulatory standards while testing raw materials using HPLC, GC, PSD, XRPD, and related techniques. You will review data, lead investigations, and contribute to method transfers and SOP development.

The role requires 5+ years in a GMP QC lab, a Chemistry-related degree, and strong analytical skills. The position involves collaboration with QA, Manufacturing, and Supply Chain in a dynamic

Qualifications

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
• Minimum 5 years of GMP-regulated QC laboratory experience focused on raw materials.
• Proficiency with HPLC, GC, PSD, XRPD and related analytical techniques.
• Strong understanding of USP/NF, EP, JP pharmacopeial standards.
• Familiarity with LIMS, Empower, and laboratory software systems.

Responsibilities

• Perform complex analytical testing of raw materials using HPLC, GC, PSD, XRPD and other techniques.
• Review and approve test data for accuracy and regulatory compliance.
• Lead investigations (OOS, OOT, Deviations) related to raw material testing.
• Author and revise SOPs, test methods, and validation protocols.
• Support method transfers, verifications, and validations.
• Collaborate with QA, Manufacturing, and Supply Chain.
• Coordinate external testing with contract labs and manage samples.
• Support and qualify raw materials through appropriate programs.
• Train and mentor junior analysts and participate in audits.

Skills

Analytical instrumentation

Regulatory standards knowledge

LIMS/Empower familiarity

Analytical thinking

Written and verbal communication

Team collaboration

Education

Bachelor's degree in Chemistry/related

Tools

HPLC

GC

PSD

XRPD

LIMS

Empower

Job description

Ocular Therapeutix, Inc. (NASDAQ:OCUL) is a biopharmaceutical company focused on the formulation, development, and commercialization of innovative therapies for diseases and conditions of the eye using its proprietary bioresorbable hydrogel-based formulation technology, ELUTYX™. Ocular Therapeutix has built a robust product pipeline of drug delivery solutions developed to reduce the complexity and burden of the current standard of care and position itself to become a leader in the ophthalmic space.

Outside of the ophthalmic realm and behind the doors of our headquarters in Bedford, MA, we strive to build a strong culture where employees can flourish and achieve their career goals. We encourage out of the box thinking, cross-functional collaboration, and creativity.

Position Summary:

The Quality Control (QC) Senior Analyst – Raw Materials is a senior-level laboratory professional responsible for the testing, qualification, and release of raw materials used in the manufacturing of pharmaceutical products. This role ensures compliance with cGMP, regulatory requirements, and internal quality standards. The Senior Analyst also mentors junior analysts, leads investigations, and supports continuous improvement initiatives.

Key Responsibilities:

• Perform complex analytical testing of raw materials (e.g., excipients, active ingredients, solvents) using techniques such as HPLC, GC, PSD, XRPD, Karl Fischer, and wet chemistry.

• Review and approve test data, ensuring accuracy, completeness, and compliance with SOPs and regulatory guidelines.

• Lead OOS (Out of Specification), OOT (Out of Trend), and Deviation investigations related to raw material testing.

• Author and revise SOPs, test methods, and validation protocols.

• Supports and executes method transfers, verifications, and validations.

• Collaborate with cross-functional teams including Quality Assurance, Manufacturing, and Supply Chain.

• Coordinate external testing with contract labs for raw materials (procuring quotes, purchase orders, shipping of samples, acquiring test results, etc.).

• Supports raw material qualification program.

• Train and mentor junior analysts and provide technical guidance.

• Participate in internal and external audits and inspections.

Qualifications:

• Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.

• Minimum 5 years of experience in a GMP-regulated QC laboratory, with a focus on raw material testing.

• Proficiency in analytical instrumentation (e.g., HPLC, GC, PSD, XRPD).

• Strong understanding of USP/NF, EP, JP, and other pharmacopeial standards.

• Familiarity with LIMS, Empower, and other laboratory software systems.

• Strong analytical thinking and problem‑solving skills.

• Excellent written and verbal communication.

• Ability to work independently and as part of a team.

Preferred Qualifications:

• Experience with compendial testing and regulatory submissions.
• Knowledge of ICH, CFR guidelines and FDA/EMA expectations.
• Experience in clean lab or continuous improvement initiatives.

Work Environment:

• Laboratory setting with exposure to chemicals and analytical instruments.
• May require occasional lifting of lab equipment or materials up to 25 lbs.
• Use of PPE and adherence to safety protocols is mandatory.

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Salary Range

$95,000—$110,000 USD

Ocular Therapeutix is an Equal Opportunity Employer and complies with all applicable federal, state, and local laws regarding nondiscrimination. Ocular Therapeutix provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, or status as a veteran. For information on how Ocular Therapeutix collects, stores, and utilizes candidate information please see our privacy policy found at https://www.ocutx.com/privacy-policy/. For the Privacy Notice for California Job Applicants, please see CCPA Applicant Notice.