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Senior Director Quality Control Jobs (NOW HIRING)

Revlon is seeking a Director, Quality Control to lead Quality Control laboratory operations at the Oxford, NC manufacturing site. This role is responsible for ensuring timely, accurate, compliant ...

Director, Quality Control

Holbrook, MA ยท On-site

$150K - $190K/yr

Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.

Director, Quality Control

Bethesda, MD ยท On-site

$100K - $150K/yr

Quality Control Director will ensure accuracy, completeness, and compliance of all audit engagements. You will review audit workpapers, financial statements, and related documentation to ensure ...

The Director, Quality Control will provide strategic leadership in managing a growing team of scientists responsible for QC-related activities and operations. This individual will be responsible for ...

Director, Quality Control

Boston, MA ยท On-site

$95 - $135/hr

Director, Quality Control (contractor) at Centessa Pharmaceuticals in Boston, MA. Location Boston, MA, United States On-site Rate Not posted Est. market $95-$135/hr Hours 30-40 hrs/week Duration ...

Director, Quality Control

Bethesda, MD ยท On-site

$100K - $150K/yr

Quality Control Director will ensure accuracy, completeness, and compliance of all audit engagements. You will review audit workpapers, financial statements, and related documentation to ensure ...

As Senior Director, Quality, you will provide strategic leadership and oversight for Repligen ... Control, Supplier Quality partnership, and Customer Quality activities. * Ensure compliance with ...

$191K - $260K/yr

As Senior Director, Quality, you will provide strategic leadership and oversight for Repligen ... Control, Supplier Quality partnership, and Customer Quality activities.Ensure compliance with ...

Showing results 21-40

Senior Director Quality Control information

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$31K

$125.6K

$213.5K

How much do senior director quality control jobs pay per year?

As of Sep 15, 2026, the average yearly pay for senior director quality control in the United States is $125,600.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,000.00 and $151,000.00 per year, depending on experience, location, and employer.

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Infographic showing various Senior Director Quality Control job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $125,600 per year, or $60.4 per hour.

Director, Quality Control

Rockville, MD โ€ข On-site

Other

This job post hasย expired 1 day ago.ย Applications are no longer accepted.


Job description

Ensures a cGMP laboratory to meet the work demand in support of manufacturing and development work as needed. Provides in depth technical and scientific advice and guidance to laboratory supervisors and analysts in the Quality Control Laboratory and Operations. Leads and empowers a team of lab leaders to ensure the laboratory is a data factory with analysts and systems that support the sampling, testing, and generation and review of data per ALCOA principles. Ensures that departmental laboratory and manufacturing related investigations are completed in a timely manner. Ensures that the Quality Control team continues to grow technically and professionally; encourages their development efforts toward excellence and a higher degree of proficiency. Provides leadership by ensuring compliance of the department with laws, regulations, guidelines, procedures, and practices governing analytical Quality Control testing, including the departmental, and company Standard Operating Procedures, and safety procedures. Ensures that processes are in place to ensure that records and technical data are accurately maintained and results well documented. Represents the Quality Control department and departmental functions on projects/committees within Samsung. Provide support of product filings with regulatory agencies (IND, BLA MAA etc). Analytical and microbiological testing and release of all components, raw materials, excipients, intermediates, active pharmaceutical ingredients (APIs), finished product and stability samples, if applicable. Sample management, including retain and stability samples as required Environmental and utilities monitoring (microbiological assurance and process control).

Educations

Bachelorโ€™s degree in a science discipline

Required Experiences

10+ years industrial experience in biopharmaceutical industry, such as Biochemistry, Analytical Chemistry, Microbiology or related field, particularly in the area of assessing physiochemical characteristics of product purity, activity and functional indicators of biological products, along with 8+ years of supervisory and managerial experiences is desired

Knowledge

Demonstrated success leading a team comprised of varying levels of technical expertise and functions. Strong verbal and written communication skills. Able to interact with peers, subordinate and senior personnel in multidisciplinary environment. Able to prioritise and decide appropriate course of actions. Effective at implementing decision. Fully versed in GMP's, NIH, ICH Guidelines, FDA and other regulatory agency requirements for validation and operations of analytical and stability functions.

Samsung Biologics is a fully integrated CDMO offering state-of-the-art contract development and manufacturing services. With proven regulatory approvals, the largest capacity, and the fastest throughput, Samsung Biologics is an award-winning partner of choice and is uniquely able to support the development and manufacturing of biologics products at every stage of the process while meeting the evolving needs of biopharmaceutical companies worldwide.

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