Associate Specialist, Chemist - Quality Control

Job Description

Are you looking for an exciting opportunity with a rapidly growing pharmaceutical manufacturer? If so, then this is the opportunity for you!

Our Quality Control group ensures every single material inside our products is manufactured, processed, tested, packaged, stored and distributed aligned with our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, external contract manufacturers and suppliers we create an interdependent global manufacturing network committed to deliver a compliant, reliable supply to customers and patients on time, every time, across the globe.

Primary Responsibilities

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Employee must show ability to perform routine assignments and develops competence by performing structured work assignments

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Ability to use existing procedures to perform routine testing

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Requires knowledge and exposure to fundamental laboratory instrumentation, theories, principles, and concepts

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Receives instruction, guidance, and direction from others and also seeks advice/information from others when addressing serious business issues that may impact other functions

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Builds and promotes the Team’s effectiveness through actions that demonstrate respect and appreciation for diverse perspectives

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Demonstrates understanding of customer needs, requirements, and expectations

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Seeks new ways to improve services to customers

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Speaks up on tough issues and expresses views and ideas at the right time while actively encouraging Team members to make suggestions and share ideas

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Works to develop new skills and abilities

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Readily accepts performance feedback and incorporates this feedback into future performance

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Assists other Team members, including helping with developmental activities

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Learns to use new problem-solving tools to surface and solve issues

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Applies general knowledge of company business developed through education and past experience

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Ability to interpret our Company Quality Policies, Guidelines and Testing Procedures for daily application

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Understands and applies regulatory/compliance requirements, including Good Manufacturing Practice (GMP), Non-Disclosure Agreement (NDA), and related regulations, and has the ability to interpret those regulations for implementation in the workplace

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Possesses a basic knowledge of theories, practices, and procedures in the Quality Control discipline, including the knowledge and understanding of pharmaceutical testing

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Active with developing technical writing capabilities and is able to compile straightforward investigations and procedures, and recommend scientifically sound corrective actions

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Possesses a basic knowledge and ability to operate lab instrumentation required to complete job responsibilities

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Uses existing procedures to perform routine testing

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Ability to independently respond to basic requests for data and trending of data

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Communicates information and asks questions to check for understanding

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Develops small scale presentations and presents to own work Team or small groups with the assistance of others

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Limited decision-making authority and works within technical guidelines/direction to achieve objectives and meet deadlines

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Accountable for technical contribution to work or project Team

Education Requirements

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Bachelor degree in Science, Engineering, or related discipline

Experience and Skills

Required

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Proficient with Microsoft Word and Excel

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Ability to work with others on a team

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Accountability for own actions, and ability to prioritize

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Knowledge of regulatory and current GMP principles

Preferred

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Operating laboratory equipment: HPLC, dissolution apparatus, KF, etc.

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Utilizing Empower | Labware/LIMS

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Execution of root cause analysis

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Background in technical writing including but not limited to: updating of standard operating procedures and writing quality notifications

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Knowledge of Tier processes

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Executing 5S principles

Salary Range: $65,100 - $102,500

Required Skills

Adaptability, Adaptability, Analytical Instrumentation, Analytical Method Development, Analytical Problem Solving, Bioburden Testing, Biopharmaceutical Industry, Chemical Analysis, Data Analysis, Disease Prevention, Global Manufacturing, GMP Compliance, Good Manufacturing Practices (GMP), Karl Fischer Titrations, Laboratory Instrumentation, Laboratory Techniques, Lab Testing Equipment, Microbiology Research, Non-Disclosure Agreements, Performance Feedback, Pharmaceutical Microbiology, Quality Control Management, Response Management, Standard Operating Procedure (SOP), Teamwork {+ 2 more}

Preferred Skills

Current Employees apply HERE

Current Contingent Workers apply HERE

US and Puerto Rico Residents Only

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$65,100.00 - $102,500.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status

Regular

Relocation

No relocation

VISA Sponsorship

No

Travel Requirements

No Travel Required

Flexible Work Arrangements

Not Applicable

Shift

1st - Day

Valid Driving License

No

Hazardous Material(s)

High Potency compounds, flammable materials

Job Posting End Date

07/1/2026

*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

Requisition ID: R403486