Quality Control Chemist I

Piramal Pharma Limited; Riverview (MI); On-site; USD 45,000 - 75,000; Full time

Job summary

An established industry player is seeking a Quality Control Chemist I to join its dynamic team in Riverview, Michigan. This entry-level role involves providing essential analytical chemistry support to ensure compliance with regulatory standards and maintain product quality. You will engage in testing raw materials, performing cleaning verifications, and documenting results meticulously. The ideal candidate will possess a Bachelor’s degree in Chemistry or Biochemistry and have a keen eye for detail. This is a fantastic opportunity to kickstart your career in the pharmaceutical industry and contribute to impactful projects in a collaborative environment.

Qualifications

• Bachelor's degree in Chemistry or Biochemistry required.
• 1 year of experience in pharmaceutical quality control preferred.

Responsibilities

• Support manufacturing by testing raw materials to meet production timelines.
• Document sample preparation and test results in compliance with regulations.

Skills

Analytical Skills

Organizational Skills

Communication Skills

Attention to Detail

Education

Bachelor’s degree in Chemistry or Biochemistry

Tools

Laboratory Analytical Instrumentation

Job description

Join to apply for the Quality Control Chemist I role at Piramal Pharma Ltd.

Job Description

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC), located in Riverview, Michigan, is seeking a qualified Quality Control Chemist I to join our Quality Control team. The Quality Control Chemist I is responsible for providing analytical chemistry support for the facility.

Requirements

• Shall adhere to all applicable regulatory requirements, including FDA, EPA, OSHA, and related safety, health and environmental procedures, policies and practices.
• Consistent support and practice of all Piramal Pharma Solutions mission, vision, and values.
• Identify and protect the original technical information as part of the company property.

Key Responsibilities

• Support manufacturing operations through the testing of raw materials and starting materials as required to meet production timelines.
• Perform cleaning verifications on multi-use equipment using approved methods.
• Test reference standards and stability samples.
• Document sample preparation, equipment set-up, and test results in laboratory notebooks or other appropriate test record forms. Verify data with second quality team member as required. Maintain all records as required to maintain compliance.
• As required, test intermediates and final products to meet production timelines/client requirements.
• Assist in the revision of documentation as required.
• Participate in quality unit projects, including but not limited to supplier certification, methods development, methods validation and training of both quality unit members as appropriate.
• Provide support in the maintenance and calibration of laboratory analytical instrumentation.
• Assist in the maintenance of the QC laboratory through routine housekeeping, as well as keeping personal bench area and desk organized.
• As required, perform routine testing on the water system (DI, ice, potable, and QC water), and prepare reports as needed.

Education/Experience

• Bachelor’s degree in Chemistry or Biochemistry or equivalent.
• One (1) year of experience in pharmaceutical quality control or equivalent is preferred.
• Familiarity with analytical testing and instrumentation.

Job Competencies

• Excellent organizational and planning skills.
• Strong written, verbal, and interpersonal communication skills.
• High attention to detail.
• Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines.

Job Conditions

The physical demands and work environment described here are representative of those that must be met by a team member to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Physical Demands:
• Frequent lifting, bending, stooping, squatting, pushing and pulling can be expected.
• Long periods of standing and walking can be expected in this position.
• This position may require long periods of sitting, typing, computer entry or looking at a computer.
• Work Environment:
• Piramal Pharma Solutions is engaged in the business of pharmaceutical research and contract pharmaceutical manufacturing. As such, all PPS staff work in or nearby either chemical/pharmaceutical research or chemical/pharmaceutical manufacturing equipment and processes.
• Potential limited exposure to hazardous chemicals.
• Personal protective equipment including safety glasses, lab coats, gloves, specialized clothing including laboratory uniform and appropriate shoes may be required in areas associated with this position.

Seniority Level

• Entry level

Employment Type

• Full-time

Job Function

• Quality Assurance
• Pharmaceutical Manufacturing