Cambridge, MA · On-site
Medical
Dental
Vision
Required Qualifications: · Validation experience in a biotech/pharmaceutical environment, specializing in Instrument or Computer System Validation · Bachelor's Degree in Engineering, Life Science ...
Quick apply
Cambridge, MA · On-site
Medical
Dental
Vision
Required Qualifications: · Validation experience in a biotech/pharmaceutical environment, specializing in Instrument or Computer System Validation · Bachelor's Degree in Engineering, Life Science ...
Cambridge, MA · On-site
Medical
Dental
Vision
Required Qualifications: · Validation experience in a biotech/pharmaceutical environment, specializing in Instrument or Computer System Validation · Bachelor's Degree in Engineering, Life Science ...
Quick apply
Cambridge, MA · On-site
Medical
Dental
Vision
Required Qualifications: · Validation experience in a biotech/pharmaceutical environment, specializing in Instrument or Computer System Validation · Bachelor's Degree in Engineering, Life Science ...
... Biotech/Biopharmaceutical industry Must be able to work in a fast paced environment Must be ... of QA/QC, validation and/or similar laboratory experience Aptitude for initiating testing ...
... Biotech/Biopharmaceutical industry Must be able to work in a fast paced environment Must be ... of QA/QC, validation and/or similar laboratory experience Aptitude for initiating testing ...
Framingham, MA · On-site
Job Title: Validation Specialist III Location: Framingham, MA Duration: 8 Months (Possible ... biotechnology industry (EU Annex 11, 21CFR Part 11, etc.). Demonstrated knowledge of GMP ...
Framingham, MA · On-site
Job Title: Validation Specialist III Location: Framingham, MA Duration: 8 Months (Possible ... biotechnology industry (EU Annex 11, 21CFR Part 11, etc.). Demonstrated knowledge of GMP ...
Bedford, NH · On-site
A master's degree is a plus, preferred. * 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required. * Sound industry knowledge of ...
Bedford, NH · On-site
A master's degree is a plus, preferred. * 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required. * Sound industry knowledge of ...
Bedford, NH · On-site
A master's degree is a plus, preferred. * 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required. * Sound industry knowledge of ...
Bedford, NH · On-site
A master's degree is a plus, preferred. * 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required. * Sound industry knowledge of ...
Waltham, MA · On-site +1
PTO
Technical Experience * 4-7 years of experience in the biotech, pharmaceutical, or medical device industry. * Strong knowledge of FDA cGMP requirements, FMEA, and riskbased validation principles.
Waltham, MA · On-site +1
PTO
Technical Experience * 4-7 years of experience in the biotech, pharmaceutical, or medical device industry. * Strong knowledge of FDA cGMP requirements, FMEA, and riskbased validation principles.
Bedford, NH · On-site
$120 - $160/hr
A master's degree is a plus, preferred. * 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required. * Sound industry knowledge of ...
Bedford, NH · On-site
$120 - $160/hr
A master's degree is a plus, preferred. * 15+ years of progressive leadership of operational validation experience in Pharmaceutical or Biotechnology industry, required. * Sound industry knowledge of ...
Boston, MA · On-site
$80 - $100/hr
PTO
Technical Experience * 3-10 years of experience within the biotech, pharmaceutical, or medical ... Validation expertise in Equipment, CSV, Method, and Process. * Protocol generation experience of ...
New
Boston, MA · On-site
$80 - $100/hr
PTO
Technical Experience * 3-10 years of experience within the biotech, pharmaceutical, or medical ... Validation expertise in Equipment, CSV, Method, and Process. * Protocol generation experience of ...
New
Bedford, MA · On-site
Medical
Dental
Vision
Life
Retirement
PTO
STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body ... The Senior Engineer/Manager, Process Validation will lead and manage various process validation ...
Bedford, MA · On-site
Medical
Dental
Vision
Life
Retirement
PTO
STOK), is a biotechnology company dedicated to restoring protein expression by harnessing the body ... The Senior Engineer/Manager, Process Validation will lead and manage various process validation ...
Tewksbury, MA · On-site
$20 - $24/hr
The job opportunity below is with one of our clients specializing in biotechnology product ... Validation Technician Location: Tewksbury, MA 01876 Duration: 12 Months Job Type: Temporary ...
Quick apply
Tewksbury, MA · On-site
$20 - $24/hr
The job opportunity below is with one of our clients specializing in biotechnology product ... Validation Technician Location: Tewksbury, MA 01876 Duration: 12 Months Job Type: Temporary ...
Boston, MA · On-site +1
PTO
The Validation Engineer will be responsible for driving overall quality performance and compliance ... Technical Experience: * 3-10 years of experience within the biotech, pharmaceutical, or medical ...
Boston, MA · On-site +1
PTO
The Validation Engineer will be responsible for driving overall quality performance and compliance ... Technical Experience: * 3-10 years of experience within the biotech, pharmaceutical, or medical ...
The Validation Engineer will be responsible for driving overall quality performance and compliance ... Technical Experience: * 3-10 years of experience within the biotech, pharmaceutical, or medical ...
Quick apply
The Validation Engineer will be responsible for driving overall quality performance and compliance ... Technical Experience: * 3-10 years of experience within the biotech, pharmaceutical, or medical ...
Boston, MA · On-site
PTO
The Validation Engineer will be responsible for driving overall quality performance and compliance ... Technical Experience: * 3-10 years of experience within the biotech, pharmaceutical, or medical ...
Boston, MA · On-site
PTO
The Validation Engineer will be responsible for driving overall quality performance and compliance ... Technical Experience: * 3-10 years of experience within the biotech, pharmaceutical, or medical ...
Bedford, NH · On-site
The Validation Engineer IV performs an array of well-defined validation activities in support of ... Technical understanding of pharmaceutical/biotechnology unit operations. * Ability to evaluate ...
Bedford, NH · On-site
The Validation Engineer IV performs an array of well-defined validation activities in support of ... Technical understanding of pharmaceutical/biotechnology unit operations. * Ability to evaluate ...
Bedford, NH · On-site
The Validation Engineer IV performs an array of well-defined validation activities in support of ... Technical understanding of pharmaceutical/biotechnology unit operations. * Ability to evaluate ...
Bedford, NH · On-site
The Validation Engineer IV performs an array of well-defined validation activities in support of ... Technical understanding of pharmaceutical/biotechnology unit operations. * Ability to evaluate ...
Boston, MA · On-site
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Boston, MA · On-site
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Boston, MA · On-site
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
Boston, MA · On-site
Job Summary The Validation Engineer III will serve as a key member of the validation team ... Minimum 4+ years of direct experience in a cGMP pharmaceutical, biotechnology, or medical device ...
$22.89 - $28
2% of jobs
$28 - $33.11
6% of jobs
$33.11 - $38.23
13% of jobs
$39.82 is the 25th percentile. Wages below this are outliers.
$38.23 - $43.34
13% of jobs
$43.34 - $48.45
11% of jobs
The median wage is $51.01 / hr.
$48.45 - $53.56
12% of jobs
$53.56 - $58.68
9% of jobs
$62.62 is the 75th percentile. Wages above this are outliers.
$58.68 - $63.79
13% of jobs
$63.79 - $68.90
13% of jobs
$68.90 - $74.02
6% of jobs
$74.02 - $79.13
3% of jobs
$22
$52
$79
For Biotech Validation jobs in Andover, MA, the most frequently searched job titles are:
Cities near Andover, MA with the most Biotech Validation job openings:
Contractor
Medical, Dental, Vision
Re-posted 27 days ago
Responsibilities:
· Provide support to the QC Analytical department for activities required to maintain CGMP status of QC Instrumentation hardware and software and to perform comparability studies for the implementation of analytical assays on new instrumentation. This scope includes QC Instruments (both portable and computer-controlled).
· Authoring Corrective & Preventive Action plans (CAPAs) for systems with long-term remediation activities, and authoring final reports for systems with short-term/completed remediation
· Performing supporting remediation work in the form of SOP revisions
· Executing change controls and validation test plans/protocols when required per remediation plans
· Responsible for the development and execution of general deliverables, such as Risk Assessments, Validation Plans, Change Impact Assessments, Design Specifications, User Requirements, Functional Requirements, Configuration Specification, Requirement Trace Matrices, IQ/OQ/UAT/PQ Protocols, and Summary Reports.
Desired Skills and Experience:
· Author, maintain, revise, and/or approve of the Validation Plan.
· Lead the resolution of deviations noted during protocol execution.
· Manage and approve vendor’s documentation as appropriate.
· Ability to impact and influence people/areas in matters related to Validation and GxP compliance.
· Ability to work in a fast-moving dynamic small company environment.
· Ability to mentor junior team members.
· Experiences in other validation areas which may include CSV qualification and Facility Equipment and Utility is a plus.
Required Qualifications:
· Validation experience in a biotech/pharmaceutical environment, specializing in Instrument or Computer System Validation
· Bachelor's Degree in Engineering, Life Science or Computer Science is required.
· Excellent working knowledge of process automation and computer system validation concepts, GAMP methodologies, CFR Part 11 Electronic Records and Signatures requirements and latest industry expectations for data integrity.
White Collar Technologies is a boutique human capital consultancy firm specializing in information technology and engineering consulting for life science sector. Our consultants serve multitude of clients within Pharmaceutical, Biotech, Medical Device, Clinical Research and Healthcare verticals.
We offer our workers Medical Dental and Vision healthcare benefits.
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