1,000+ matching jobs for “Senior Product Specialist”

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Cardinal Health

Senior Specialist, Quality Control Chemist II (2nd shift)

IN-Indianapolis-Theranostics Commercial

Pay posted by employer$68,500–$88,020

… timely and thorough inspections and analysis of incoming materials, Drug Substance, In-Process and Drug Product samples. Performs investigations, deviations, change controls and CAPAs. Execute method verification, …

Added Oct 27, 2026

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Johnson & Johnson

Senior Neuroscience Sales Specialist (Spokane, WA) – Johnson & Johnson Innovative Medicine

Spokane, Washington, United States

Full time
Regular

We are searching for the best talent for a Senior Neuroscience Sales Specialist to support clients and patients in the Spokane, WA territory. About …

Added Oct 15, 2026

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Merck (MSD)

Specialist, Bioprocess Engineer

USA - Delaware - De Millsboro

Pay posted by employer$87,300–$137,400

… Because when it comes to animal health, no one sees it like we do. As a BioTechnology Solutions (BTS) Specialist and manufacturing process engineer , you will be part of a world-class team within Animal Health, …

Added Oct 15, 2026

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Danaher

Senior Commercial Quality Assurance Specialist - French Speaking - 12 Month Contract

Morocco +2 locations

Contract

Regulatory Submissions & Product Registrations Prepare and manage regulatory submissions for African countries, including initial …

Added Oct 30, 2026

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Gilead Sciences

Sr Field Activation Specialist, HIV Prevention - CA Central Valley

United States - Field +3 locations

Full time
Regular

Pay posted by employer$133,195–$172,370

… deliver therapies that will improve the lives of patients with life-threatening illnesses worldwide. As a Senior Field Activation Specialist within Gilead's HIV Prevention Team, you will represent Gilead's products and …

Added Oct 15, 2026

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Johnson & Johnson

Senior Source Regulatory Compliance Specialist, Supplier Auditor (m/f/d)

Umkirch, Germany

Full time
Regular

… appropriate time and subject to any necessary consultation processes. The Sr. Source Regulatory Compliance Specialist is responsible for planning, executing, and supporting supplier audits and related regulatory compliance …

Added Oct 15, 2026

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Cencora

Senior Field Reimbursement Specialist- Cell and Gene Therapy/Rare Disease

Remote, USA

Full time

Pay posted by employer$93,500–$187,000

. T he Sr Field Reimbursement Specialist (FRS) will plan and engage with health systems, hospitals, academic medical centers, authorized treatment …

Added Oct 27, 2026

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Nike

Lead Technical Product Manager Finance, ITC

Karnataka, India

… to deliver enterprise-grade finance planning solutions. WHO WE ARE LOOKING FOR We are looking for a Lead Product Manager to shape and drive the product strategy, roadmap, and business outcomes for Nike's Enterprise …

Added Oct 27, 2026

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Danaher

Technical Specialist II

Inashiki-gun, Ibaraki, Japan

Regular

… OLED screens to paper—everyday Pall is there, helping protect critical operating assets, improve product quality, minimize emissions and waste, and safeguard health. For the exponentially curious, Pall is a place …

Added Oct 15, 2026

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Johnson & Johnson

Snr Clinical & Sales Specialist

North Ryde, New South Wales, Australia

Full time
Regular

… on their journey to wellness. The Opportunity An opportunity has become available for a results driven Senior Clinical Specialist to join our Electrophysiology Team in Sydney . The overall responsibility of this role …

Added Oct 15, 2026

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Bristol-Myers Squibb

Senior Therapeutic Area Specialist, Oncology- Eastern NC/ Norfolk, VA

Greenville - NC - US +2 locations

Full time
Regular

Pay posted by employer$144,500–$175,100

… HCPs and ensures medical accuracy. Conducts in-office presentations (e.g., lunch and learns) and discusses product-related scientific information with HCPs that is consistent with label. Organizes external speaker …

Added Oct 15, 2026

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Thermo Fisher Scientific

Principal Regulatory Affairs Specialist

São Paulo, São Paulo, Brazil

Join Us as a Principal Regulatory Affairs Specialist – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 27, 2026

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Bristol-Myers Squibb

Senior Institutional Mental Health Account Specialist, Neuroscience - COBENFY - Chicago, IL

Chicago - IL - US

Full time
Regular

Pay posted by employer$147,560–$178,808

… first ever treatment to target muscarinic receptor circuits for schizophrenia. The Mental Health Account Specialist team will call on the providers and care team members specifically at Community Mental Health Centers, …

Added Oct 15, 2026

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Regeneron Pharmaceuticals

Compliance Specialist, External Manufacturing

RENSS - TECH VALLEY

Full time
Regular

Pay posted by employer$62,355–$128,700

… to develop life-changing medicines for people with serious diseases. We are seeking to fill a Compliance Specialist position within the External Manufacturing team. This role is responsible for operations support and …

Added Oct 16, 2026

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Comfort Systems USA

Indoor Air Quality Specialist

Missoula, MT (TempRight HQ)

Full time
Regular

The IAQ & Duct Cleaning Specialist is responsible for improving the health, safety, comfort, and efficiency of residential and commercial HVAC …

Added Oct 27, 2026

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Air Products & Chemicals

Onsite Sales Specialist

Hsinchu, Taiwan, Taiwan

Full time

… Project Delivery, Quality, Logistics, Distribution and BDS to form the bidding strategy and tactics. Obtain senior management approval through OSDs and Firm Pricing Approval. Good communication with customers and negotiate …

Added Nov 3, 2026

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Regeneron Pharmaceuticals

Temp - QA Specialist

Limerick, Munster, Ireland

Full time
Temporary

… coaching, and mentoring on QA processes, procedures, and standards Performing activities related to product disposition and release, including review of manufacturing records and supporting documentation Reviewing …

Added Oct 16, 2026

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Regeneron Pharmaceuticals

Temp QA Specialist

Limerick, Munster, Ireland

Full time
Temporary

Added Oct 16, 2026

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Bristol-Myers Squibb

Senior Therapeutic Area Specialist, Oncology- Salt Lake City/Boise

Salt Lake City - UT - US +1 location

Full time
Regular

Pay posted by employer$144,500–$175,100

Added Oct 15, 2026

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Bristol-Myers Squibb

Senior Therapeutic Area Specialist, Cardiovascular Community - Upper Manhattan E

MANHATTAN - NY - US

Full time
Regular

Pay posted by employer$124,090–$150,370

Added Oct 15, 2026

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Cardinal Health

Senior Specialist, Quality Control Chemist II (2nd shift)

IN-Indianapolis-Theranostics Commercial

Pay posted by employer$68,500–$88,020

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Qualifications · employer excerpt

Bachelor’s degree or previous work experience in a similar role or related field chemistry, or biology preferred.
2+ years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred.
Has general knowledge of GDP documentation practices and requirements
Has experience in authoring a variety of forms of documentation such as SOPs, Change Controls, CAPAs, Deviations and Laboratory Investigations.
Must work well with others and understand how to be successful in a team environment.

4 more in the full description below.

About this opportunity

Original employer description

What Quality Control contributes to Cardinal Health
Quality develops and implements quality policies, procedures, and processes to ensure products and services comply with regulatory standards and specifications.

Quality Control is responsible for the analysis or inspection of materials, components, products or processes for compliance with specifications and standards.

Responsibilities

Reports to Supervisor, Quality Control (Chemistry)
Ensures timely and thorough inspections and analysis of incoming materials, Drug Substance, In-Process and Drug Product samples.
Performs investigations, deviations, change controls and CAPAs.
Execute method verification, validation and/or transfer protocols.
Perform stability testing in alignment with stability protocol(s) at the prescribed cadence.
Authors standard operating procedures, analytical method worksheets, forms and other documents as necessary and applicable.
Demonstrates detail-oriented attention in all facets of responsibilities.
Performs visual assessment and analytical evaluation or test of products or processes.
Demonstrates knowledge of testing methods, product usage, and applicable regulations and standards.
Adheres to established policies and procedures.
Establishes test methodology.
May train others on SOPs, PROTOCOLs, instruments and quality guidelines.
May execute analytical equipment qualification protocols or computer system validation test scripts.
Aligns work priorities with immediate supervisor/management.
Gain awareness of other departments at site. Seek to understand the functions of those departments and the points of interaction between Quality Control and your role.
Exhibits Cardinal Health's high ethical standards and code of conduct.
Performs special projects or tasks as necessary based on skill set and/or development goals and business needs.
Performs other job duties as assigned.

Qualifications

Bachelor’s degree or previous work experience in a similar role or related field chemistry, or biology preferred.
2+ years of relevant work experience working with 21 CFR 210, 211 in the FDA regulated industry (Pharmaceutical or Medical Device) preferred.
Has general knowledge of GDP documentation practices and requirements
Has experience in authoring a variety of forms of documentation such as SOPs, Change Controls, CAPAs, Deviations and Laboratory Investigations.
Must work well with others and understand how to be successful in a team environment.
Must be detail oriented, organized, able to multitask, a self-starter, and self-motivated.
Must be proficient in Microsoft Word and Microsoft Excel and possess strong technical writing skills.
Demonstrated success in collaborating with people and working on a team.
Strong communications skills.

Location

Onsite in Indianapolis, IN

Performance Expectations

Demonstrates a commitment to the organization’s mission, vision and values supporting organizational decisions and behaviors. Contributes to the development and implementation of systems and processes ensuring strategic goal attainment.
Works as part of a team with others and shows respect and values diversity toward others.
Takes actions to continually improve quality and safety in daily work. Actively participates in improving work processes to meet and exceed expectations. Identifies opportunities for improvement based on process observations, outcome measures, and feedback.
Reports errors in a timely and appropriate manner. Takes initiative and is accountable for areas of responsibility meeting regulatory requirements including but not limited to maintaining required trainings as appropriate to position requirements.
The ability to act calmly and patiently when working under pressure and/conditions of stress. Maintains integrity, composure, communicates with honesty, transparency, clarity and promotes alternative perspectives.

Physical/ Mental Requirements

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; balance; stoop, kneel, crouch or crawl; talk or hear; and taste or smell. The employee must occasionally lift or move up to 25 pounds. Specific vision abilities required by the job include close vision, distance vision, color vision, peripheral vision, depth perception and the ability to adjust focus.

Work Environment

The primary work environment consists of a professional office environment within a radiopharmaceutical manufacturing facility, the materials warehouse as well as the laboratory setting.
The facility is operated under well-controlled and closely monitored conditions that are regulated by both State and Federal agencies, and that are enforced by the corporate internal quality and regulatory groups. Each staff member will receive specific training in keeping radiation exposures within regulatory guidelines and he/she will be routinely monitored for their exposure to radiation. Noise levels are considered low to moderate.
This role works second shift (M-F, 3:30 p.m. - Midnight).

What is expected of you and others at this level

This role will perform analysis of Incoming Materials, Drug Substance, In-Process and Drug Product samples.
This role will execute method verification, validation and/or transfer protocols.
This position will perform stability testing in alignment with stability protocol(s) at the prescribed cadence.
This position may execute analytical equipment qualification protocols or computer system validation test scripts.
Exhibits Cardinal Health's high ethical standards and code of conduct.
Approaches work situations with a positive and energizing style.
Aligns work priorities with immediate supervisor/management.
Gain awareness of other departments at site. Seek to understand the functions of those departments and the points of interaction between Quality Control and your role.
Exhibit professional conduct and respect for others.

Anticipated salary range: $68,500.00-$88,020.00

Bonus eligible: No

Benefits: Cardinal Health offers a wide variety of benefits and programs to support health and well-being.

Medical, dental and vision coverage
Paid time off (Untracked)
Health savings account (HSA)
401k savings plan
Access to wages before pay day with myFlexPay
Flexible spending accounts (FSAs)
Short- and long-term disability coverage
Work-Life resources
Paid parental leave
Healthy lifestyle programs

Application window anticipated to close: 12/5/2026 *if interested in opportunity, please submit application as soon as possible.

The salary range listed is an estimate. Pay at Cardinal Health is determined by multiple factors including, but not limited to, a candidate’s geographical location, relevant education, experience and skills and an evaluation of internal pay equity.

Cardinal Health supports an inclusive workplace that values diversity of thought, experience and background. We celebrate the power of our differences to create better solutions for our customers by ensuring employees can be their authentic selves each day. Cardinal Health is an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, ancestry, age, physical or mental disability, sex, sexual orientation, gender identity/expression, pregnancy, veteran status, marital status, creed, status with regard to public assistance, genetic status or any other status protected by federal, state or local law.

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Keywords also found in description

Quality Function

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