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 III analyzes process samples as received and performs non-routine analysis as requested. She/he analyzes 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. Acts as a mentor for other technicians.Job Description
ESSENTIAL FUNCTIONS:
- Ability to proficiently perform all functions of a Quality Tech II.
- Must be completely trained and proficient in all rotating areas of the QC Lab, i.e., PAP Controls, APAP Controls, and Finished Lot testing.
- Performs in process testing for our internal customers.
- Performs finished goods, returned goods, and stability testing for our external customers as needed.
- Performs testing on all bulk raw materials as needed.
- Performs specified analysis on bulk raw materials, all process control samples and and reports results in a timely manner by telephone or computer entry using approved written procedures and proper laboratory techniques.
- Performs specified analysis on all finished goods and non-routine customer tests using approved written procedures and laboratory techniques as needed.
- Maintains accurate and precise records of all laboratory analysis using appropriate Mallinckrodt recordkeeping system. Demonstrates good documentation skills as a documentation reviewer.
- Prepares all standards and reagents needed for proper execution of analytical methods and procedures.
- Troubleshoots and performs routine maintenance on laboratory instrumentation and takes ownership of continued education with regard to instrument maintenance and troubleshooting.
- Prioritizes and plans workload and team assignments to meet all internal and external customer needs for maximum efficiency and accuracy.
- Takes on a leadership role. Point of contact for plant and QC/QA management. Ensures that the lab runs smoothly and all required testing is being addressed by staffing areas appropriately according to technician training.
DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:
- Other duties as assigned with or without accommodation.
- Assists in any non-routine analytical work needed to solve plant problems.
- Works on solving problems and implementing improvements in a teaming environment.
- Demonstrates advanced problem solving skills to analyze and help complete failure investigations and testing problems.
- Aids in performing any 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.
- Participates in customer audits and Lab tours.
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:
2 – 4 years laboratory experience in a pharmaceutical manufacturing operation
Must have at least 2 years QC Lab experience, trained and competent in all areas, i.e., PAP Controls, APAP Controls Lab, and Finished Lot testing.
Working knowledge of cGMP required.
Preferred Skills/Qualifications:
Other Skills/Competencies:
Must be able to comprehend and independently carry out written procedures, record results and observations, and perform mathematical calculations.
Requires familiarity with all laboratory procedures and equipment and an understanding of instrument operations.
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
Sound and correct technical judgments are required during routine analysis.
Strong computer skills.
RELATIONSHIP WITH OTHERS/ SCOPE:
- Reports to Quality Control Manager.
- Frequent interactions 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. Inability to work with set priorities can result in process delays and/or missed shipping commitments.
- 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.
- Laboratory technicians are responsible for communicating any uncompleted work to the next shift, as well as any immediate priorities. No supervisory responsibilities are assigned to Quality Tech III, but they do provide examples of proper technique in training new employees as assigned.
- Majority of work is performed independently without direct supervision.
- 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.
Skills Required
- Associate of Science, Bachelor of Science, or equivalent life science degree; appropriate experience may substitute
- 2–4 years of laboratory experience in a pharmaceutical manufacturing operation
- At least 2 years of quality control laboratory experience
- Training and competency in PAP Controls, APAP Controls Lab, and Finished Lot testing
- Working knowledge of cGMP
- Ability to independently comprehend and carry out written procedures
- Ability to record results and observations and perform mathematical calculations
- Familiarity with laboratory procedures, equipment, and instrument operations
- Ability to differentiate colors and pass a color-vision test, with permitted corrective eyewear if needed
- Strong computer skills
- Ability to work rotating 12-hour shifts and occasional overtime
- Ability to wear required personal protective equipment, including hard-hat, steel-toe shoes, and safety glasses
Endo Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Endo and has not been reviewed or approved by Endo.
-
Fair & Transparent Compensation — Pay is considered competitive to good across many roles, with total compensation in commercial positions strengthened by sizable bonus/OTE when targets are met. Subsidiary experiences within the group also point to good compensation, reinforcing a generally positive pay story.
-
Healthcare Strength — Core medical, dental, and vision coverage is strong, complemented by virtual care, disease‑management programs, and a health advocate service. Health coverage is described as good, adding perceived value beyond base pay.
-
Retirement Support — A 401(k) plan provides a company match up to 4%, supporting employees’ long‑term savings. Current materials outline the matching formula clearly for prospective comparisons.
Endo Insights
What We Do
At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.







