Quality Control Chemist

PPL Pharma Solutions Riverview LLC; Riverview (MI); On-site; USD 52,000 - 76,000; Full time

Job summary

Piramal Pharma Solutions’ HPAPI Research and Manufacturing facility (Ash Stevens, LLC), in Riverview, Michigan, is seeking a Quality Control Chemist I to join the QC team. The role provides analytical chemistry support and requires a Bachelor’s in Chemistry or Biochemistry with relevant experience.

Ideal candidates have strong attention to detail, good communication skills, and the ability to work independently to meet production timelines.

Qualifications

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

Responsibilities

• Support QC operations by testing raw materials and in-process samples.
• Perform verifications and document results in lab records.
• Maintain equipment calibration and laboratory housekeeping.
• Assist in methods development and validation activities.
• Contribute to documentation updates and training as needed.

Skills

Organizational skills

Communication skills

Attention to detail

Analytical skills

Independent work

Education

Bachelor’s degree in Chemistry or Biochemistry

Job description

Company Overview

Be the First to Apply Division Piramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com

Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group. PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.

Job Title

Quality Control Chemist

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 II is responsible for providing analytical chemistry support for the facility.

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. undefined 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.