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Skills: Quality control, Laboratory analysis, Chemical testing, Instrumental analysis, cGMP
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MBP (McDonough Bolyard Peck)
Engineer (Entry-Level) (Full-Time)
Raleigh, North Carolina, United States · On-site
$66k–$79k/yr
Entry level
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Full-time
associate degree, bachelor degree
Posted 9d ago
~40 hrs/week
Responsibilities
The Quality Tech II analyzes process samples, finished goods, and raw materials using chemical and instrumental methods to ensure quality standards. They are also responsible for maintaining accurate laboratory records, troubleshooting instrumentation, and participating in failure investigations.
Requirements
Candidates should possess an Associate or Bachelor of Science degree in a life science field and 1-3 years of pharmaceutical laboratory experience. Proficiency in cGMP and the ability to work a rotating 12-hour shift schedule are required.
Full job description
Why Us?
At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.
Job Description Summary
The Quality Tech II analyzes process samples as received and performs non-routine analysis as requested. She/he will analyze finished goods and raw materials by chemical, physical, and instrumental means to ensure quality as needed. She/he will typically work on a rotating shift schedule.
Job Description
ESSENTIAL FUNCTIONS:
Performs in process testing for internal customers.
Performs finished goods, returned goods, and stability testing for external customers as needed.
Performs specified analysis on all process controls samples and reports in a timely manner by telephone or computer entry using approved written procedures and proper laboratory techniques.
Performs specified analysis on all finished goods using approved written procedures and proper laboratory techniques as needed.
Maintains accurate and precise records of all laboratory analysis using appropriate Mallinckrodt recordkeeping system.
Troubleshoots and performs routine maintenance on laboratory instrumentation.
Prepares all standards and reagents needed for proper execution of analytical methods and procedures.
Prioritizes and plans workload to meet all internal and external customer needs for maximum efficiency and accuracy.
DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:
Assists in any non-routine analytical work needed to solve plant problems.
Works on solving problems and implementing improvements in a teaming environment.
Uses problem solving skills to help with failure investigations and testing problems.
Aids in performing any non-routine quality control related tasks such as resampling, raw material testing, and performing analysis needed to validate methods and equipment.
Participates in a certified 5S Workplace System to ensure good housekeeping and organization.
Assists with training others as needed.
Other duties as assigned with or without accommodation.
MINIMUM REQUIREMENTS:
Education:
Associates of Science (AS) or Bachelor of Science (BS) or equivalent life science degree preferred. Appropriate experience may be a suitable replacement for degree.
Experience:
1 – 3 years laboratory experience in a pharmaceutical manufacturing operation preferred. Working knowledge of cGMP is a plus.
Expected Skills/Qualifications:
Other Skills/Competencies:
Must be able to perform basic mathematical calculations.
Familiarity with basic laboratory procedures, equipment, and computer key punching.
Sound and correct technical judgments are required during routine analysis.
High degree of concentration is required.
Ability to differentiate colors, as demonstrated by passing a test designed to identify color blindness (such as the Ishihara test). If testing criteria are not met with
uncorrected vision, the use of color correcting glasses may be used as long as testing criteria are met while using them.
Functional/Technical Skills, Priority Setting, Written Communication
Customer Focus, Organizing
RELATIONSHIP WITH OTHERS/ SCOPE:
Laboratory technicians are responsible for communicating any uncompleted work to the next shift, as well as any immediate priorities.
Majority of work is performed independently without direct supervision. Non-routine results, observations, or analytical requests are brought to the attention of the appropriate management personnel.
Reports to Quality Testing and Release Manager.
Frequent interact with operators, engineers, and Quality management for reporting routine analytical results. Communication may be though radio, telephone, email, or in person.
Incorrect or inaccurate analyses can result in possible shipment of reject drug items to Mallinckrodt customers.
Customer-requested specifications and Mallinckrodt methods of analysis are considered confidential for marketing purposes.
Ability to understand the timely nature of work, quick reporting of results, and fast changing of priorities are necessary to complete assigned tasks. Laboratory employees must be able to work effectively under these conditions.
Completes all required Compliance trainings in a timely manner.
WORKING CONDITIONS:
Most work is performed in a well-equipped analytical laboratory complete with fume hoods, laboratory benches, analytical glassware, and instruments.
Boxes of solvents, compressed gas cylinders, old records, and reserve samples are stored in areas outside the laboratory and may require lifting and transporting to the laboratory area.
Exposure to fugitive emissions of chemicals typical for chemical operations.
Normal dexterity is required for routine handling of laboratory glassware and instruments. Colors must be well-visualized and slight differences in volumes of liquids in appropriate glassware distinguished.
Must be able to wear the required personal protective equipment (PPE), such as hard-hat, steel-toe shoes, safety glasses, and other equipment as deemed necessary by EH&S, leadership team, corporate, or safety guidelines for the position.
Must be able to work a rotating12 hour shift schedule of (7pm-7am / 7am-7pm) in addition to occasional overtime as needed.
DISCLAIMER:
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position.
EEO Statement:
We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.
Endo combined with Mallinckrodt Pharmaceuticals in 2025 to better serve customers and improve outcomes for the patients we support.
From this union, we established two focused, standalone companies:
– Keenova Therapeutics, a branded therapeutics business
– Par Health, a generics and sterile injectables business
To learn more, follow Keenova and Par Health on LinkedIn and visit keenova.com and parhealth.com.
Offices: Malvern, US
Health CareBiotechnologyPharmaceuticalBiotech & PharmaceuticalsPharmaceutical and biotechnology
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