Job Overview
Compensation
Hourly
Range $18.25 - $25.25
Work Schedule
Day Shifts
Benefits
Medical insurance
Vision Insurance
Dental Insurance
Paid Time Off
Holidays
Life insurance
401k Company Match
Professional development programs
Job Description
Almac Group, Inc. is a renowned, award-winning drug development solutions provider that stands at the forefront of the pharmaceutical industry. With a legacy spanning over 50 years, this privately owned organization has grown organically, now employing approximately 5,600 highly skilled personnel worldwide. The company’s US headquarters is located in Souderton, Pennsylvania, complemented by additional operations scattered across the US and Europe. Almac Group takes pride in its mission of 'Partnering to Advance Human Health,' which resonates not just as a tagline but as an intrinsic part of their corporate culture and operational philosophy.
Founded on principles of innovation and quality, Almac Group serves a vital role in the pharmaceutical industry by supporting drug development from research through to commercialization. Their comprehensive services encompass a wide range of capabilities including drug substance and drug product manufacturing, clinical trial materials management, and commercial packaging and distribution. These services are backed by robust quality systems and compliance with cGMP (current Good Manufacturing Practices) as well as other regulatory requirements to ensure the highest standards are met. Join a team that values diversity, inclusion, and continuous learning, offering a workplace where every employee is given the opportunity to contribute to advancing healthcare globally.
The QC Inspector position based at Almac's Souderton, PA facility involves critical responsibilities focused on maintaining the quality standards expected within the pharmaceutical manufacturing environment. This full-time role operates on a 7am to 3pm schedule designed to support key operational activities. The QC Inspector will be tasked with auditing and inspecting operational activities and outputs for adherence to cGMPs, SOPs, and other established quality controls. This role is essential to the validation and verification processes throughout manufacturing, packaging, and quality assurance workflows, ensuring that products leaving the facility meet stringent quality criteria.
Key duties include conducting in-process quality checks on products, processes, and room layouts, verifying calibration of critical equipment such as balances and scales, and performing set-up inspections to set accept/reject standards for batches. The QC Inspector will engage closely with other departments including Quality, Incoming Goods, Project Services, and Logistics to resolve quality issues and enhance operational compliance. The role also encompasses cold condition inspections within 2-8°C environments, emphasizing the need for attention to detail and adherence to safety protocols. Additionally, this role supports the training of personnel in cGMP, SOP, and job skills, fostering a culture of quality and continuous improvement throughout Almac Clinical Services. This opportunity offers meaningful work in a dynamic, regulated environment that prioritizes quality and rigorous standards, contributing significantly to the manufacturing and packaging process of critical pharmaceutical products.
Founded on principles of innovation and quality, Almac Group serves a vital role in the pharmaceutical industry by supporting drug development from research through to commercialization. Their comprehensive services encompass a wide range of capabilities including drug substance and drug product manufacturing, clinical trial materials management, and commercial packaging and distribution. These services are backed by robust quality systems and compliance with cGMP (current Good Manufacturing Practices) as well as other regulatory requirements to ensure the highest standards are met. Join a team that values diversity, inclusion, and continuous learning, offering a workplace where every employee is given the opportunity to contribute to advancing healthcare globally.
The QC Inspector position based at Almac's Souderton, PA facility involves critical responsibilities focused on maintaining the quality standards expected within the pharmaceutical manufacturing environment. This full-time role operates on a 7am to 3pm schedule designed to support key operational activities. The QC Inspector will be tasked with auditing and inspecting operational activities and outputs for adherence to cGMPs, SOPs, and other established quality controls. This role is essential to the validation and verification processes throughout manufacturing, packaging, and quality assurance workflows, ensuring that products leaving the facility meet stringent quality criteria.
Key duties include conducting in-process quality checks on products, processes, and room layouts, verifying calibration of critical equipment such as balances and scales, and performing set-up inspections to set accept/reject standards for batches. The QC Inspector will engage closely with other departments including Quality, Incoming Goods, Project Services, and Logistics to resolve quality issues and enhance operational compliance. The role also encompasses cold condition inspections within 2-8°C environments, emphasizing the need for attention to detail and adherence to safety protocols. Additionally, this role supports the training of personnel in cGMP, SOP, and job skills, fostering a culture of quality and continuous improvement throughout Almac Clinical Services. This opportunity offers meaningful work in a dynamic, regulated environment that prioritizes quality and rigorous standards, contributing significantly to the manufacturing and packaging process of critical pharmaceutical products.
Job Requirements
- High school diploma or equivalent
- 1+ year of relevant manufacturing, packaging, or quality assurance/quality control experience
- Ability to perform inspections in cold environments (2-8°C)
- Strong attention to detail and adherence to quality standards
- Ability to follow cGMP, SOPs, and company procedures
- Effective communication skills to interact with multiple departments
Job Qualifications
- High school diploma or equivalent
- 1+ year of manufacturing, packaging, or quality assurance/quality control experience
- Knowledge of function and purpose of quality control within a manufacturing environment
- Associates or bachelor’s degree with science background preferred
- Experience in pharmaceutical manufacturing, packaging, or quality assurance/quality control preferred
- Knowledge of current pharmaceutical Good Manufacturing Practices preferred
Job Duties
- Complete in-process quality checks on products, processes, room layout, and safety to ensure compliance with GMP and Almac Clinical Services procedures
- Perform set-up inspections, including setting accept/reject standards, to establish quality criteria for each batch
- Complete area and equipment clear/clean inspections
- Perform verification checks of documents and clinical material upon completion of packaging activities
- Inspect material/operations within cold conditions (2-8°C)
- Check calibration of balances and scales used in Almac Clinical Services
- Interact with Quality, Incoming Goods, Project Services, and Logistics personnel to address quality issues
- Assist in cGMP, SOP, and job skill training of quality control and other Almac Clinical Services personnel
Job Criteria
Experience
No experience required
Job Location
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