Quality Compliance/Labeling Specialist Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology ...
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Quality Compliance/Labeling Specialist Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology ...
Quick apply
Quality Compliance/Labeling Specialist Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology ...
Quality Compliance/Labeling Specialist Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology ...
Quick apply
Quality Compliance/Labeling Specialist Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology ...
Cupertino, CA · On-site
$62 - $67/hr
Knowledge of domestic and international medical device regulatory requirements for product labeling and unique device identification (e.g. 21 CFR 801 and EU MDR). * Knowledge of quality management ...
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Cupertino, CA · On-site
$62 - $67/hr
Knowledge of domestic and international medical device regulatory requirements for product labeling and unique device identification (e.g. 21 CFR 801 and EU MDR). * Knowledge of quality management ...
Irvine, CA · On-site
Review and approve labeling to ensure compliance with ISO 15223-1 (medical device symbols), ISO 20417 (information supplied by the manufacturer), ISO 5840 (cardiovascular implant labeling), and EU ...
Irvine, CA · On-site
Review and approve labeling to ensure compliance with ISO 15223-1 (medical device symbols), ISO 20417 (information supplied by the manufacturer), ISO 5840 (cardiovascular implant labeling), and EU ...
Belmont, MA · On-site
$50 - $75/hr
Freelance Medical Writer We are seeking an experienced Freelance Medical Writer to join our team ... Pharmaceutical, biotech, medical device sales training experience a plus * At Custom Learning ...
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Belmont, MA · On-site
$50 - $75/hr
Freelance Medical Writer We are seeking an experienced Freelance Medical Writer to join our team ... Pharmaceutical, biotech, medical device sales training experience a plus * At Custom Learning ...
Irvine, CA · On-site
$82K/yr
Review and approve labeling to ensure compliance with ISO 15223-1 (medical device symbols), ISO 20417 (information supplied by the manufacturer), ISO 5840 (cardiovascular implant labeling), and EU ...
Irvine, CA · On-site
$82K/yr
Review and approve labeling to ensure compliance with ISO 15223-1 (medical device symbols), ISO 20417 (information supplied by the manufacturer), ISO 5840 (cardiovascular implant labeling), and EU ...
Irving, TX · On-site
... Medical device Labeling and packaging re-design and test methods to improve label readability, barcode placement, and manufacturing efficiency -Participate in investigations related to labeling ...
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Irving, TX · On-site
... Medical device Labeling and packaging re-design and test methods to improve label readability, barcode placement, and manufacturing efficiency -Participate in investigations related to labeling ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
Covington, GA · On-site
The WSL will be able to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR ...
Covington, GA · On-site
The WSL will be able to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Medtronic ...
This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Medtronic ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
The WSL will beable to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR 801 ...
Covington, GA · On-site
The WSL will be able to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR ...
Covington, GA · On-site
The WSL will be able to develop, design, and release medical device product labeling with the support of cross-functional business units that comply with global regulatory requirements such as CFR ...
This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Structural ...
This position will be a subject matter expert in Medical Device labeling regulations and standards. They will be responsible for planning, development and execution of product labeling for Structural ...
Dallas, TX · On-site
$21 - $22/hr
Medical Device Assembler The assembler works in a fast-paced medical device warehouse, handling the ... Prepare outgoing shipments by picking, packing, labeling, and staging products according to ...
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Dallas, TX · On-site
$21 - $22/hr
Medical Device Assembler The assembler works in a fast-paced medical device warehouse, handling the ... Prepare outgoing shipments by picking, packing, labeling, and staging products according to ...
Irving, TX · On-site
Execute Medical device Labeling and packaging re-design and test methods to improve label readability, barcode placement, and manufacturing efficiency * Participate in investigations related to ...
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Irving, TX · On-site
Execute Medical device Labeling and packaging re-design and test methods to improve label readability, barcode placement, and manufacturing efficiency * Participate in investigations related to ...
... label finished medical devices accurately • Complete production records and work order documentation while maintaining a clean work area Candidates for Medical Device Assembler must meet the ...
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... label finished medical devices accurately • Complete production records and work order documentation while maintaining a clean work area Candidates for Medical Device Assembler must meet the ...
$23.52 is the 25th percentile. Wages below this are outliers.
$14.90 - $25.57
31% of jobs
The median wage is $32.14 / hr.
$25.57 - $36.23
31% of jobs
$36.23 - $46.90
4% of jobs
$56.23 is the 75th percentile. Wages above this are outliers.
$46.90 - $57.56
10% of jobs
$57.56 - $68.23
9% of jobs
$68.23 - $78.89
5% of jobs
$78.89 - $89.55
0% of jobs
$89.55 - $100.22
8% of jobs
$100.22 - $110.88
0% of jobs
$110.88 - $121.55
0% of jobs
$121.55 - $132.21
1% of jobs
$14
$47
$132
$57 - $67/hr
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 9 days ago
Adecco Healthcare & Life Sciences is hiring for a notable global medical device organization recognized for its innovation in consumer and clinical technology products, quality-driven design standards, and strong commitment to global regulatory compliance.
This is a contract opportunity for a Labeling Specialist supporting global product labeling, Instructions for Use (IFU) development, and regulatory compliance activities across domestic and international markets.
Pay: Up to 67/hr depending on relevant experience level
Duration: 6 months temp to hire
Location: CUPERTINO, CA
Join a cross-functional regulatory and quality team responsible for ensuring accurate, compliant, and globally aligned product labeling for medical devices. In this role, you will support the creation, review, and maintenance of Instructions for Use (IFUs), marketing claims, and labeling documentation while ensuring adherence to global regulatory requirements.
This position plays a key role in maintaining compliance with evolving domestic and international medical device labeling standards while collaborating closely with Regulatory Affairs, Quality, Engineering, and Marketing teams.
Lead the development and maintenance of Instructions for Use (IFUs) ensuring compliance with global regulatory requirements
Review and approve product labeling to ensure accuracy, completeness, and regulatory alignment
Manage labeling-related marketing claims and coordinate cross-functional approvals
Support internal review processes for marketing and post-market labeling materials
Establish and maintain systems for physical and electronic labeling controls
Ensure labeling documentation remains compliant with global standards and evolving regulatory requirements
Partner with Regulatory Affairs to incorporate country-specific labeling requirements and translations for international markets
Participate in design control and change control processes related to product updates, enhancements, and regulatory changes
Bachelor’s degree or equivalent relevant experience
2–5 years of experience in medical device labeling or regulatory labeling support
Strong understanding of global medical device labeling regulations, including 21 CFR 801 and EU MDR
Knowledge of Quality Management Systems (QMS), including design control, document control, and regulatory approval processes
Excellent written and verbal communication skills
Strong interpersonal skills with experience working across multiple cross-functional teams
Highly organized with strong attention to detail and time management skills
Ability to work independently and manage multiple priorities
Technical writing experience preferred
Adecco Healthcare & Life Sciences connects talented professionals with leading organizations across the medical device, biotechnology, pharmaceutical, and diagnostics industries. We specialize in both contract and direct hire opportunities that support career growth and long-term development.
We offer:
Access to top-tier medical device and life sciences opportunities
Weekly pay options for applicable roles
Comprehensive medical, dental, vision, and 401(k) benefits
Dedicated recruiter support throughout your assignment
Opportunities across global, regulated life sciences organizations
Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
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