Hello Connections! Pharmatek is actively hiring for Remote opportunity for Informatica developer Requirements • CDGC experience along with customization of data governance. Data Quality/MDM is less relevant • Write design documents and coordinate with cross functional groups • Able to work independently and drive the conversations and requirements • familiar with git and common software development practices around source control Interested candidates apply here: https://lnkd.in/gC2T8sJC
Pharmatek
IT Services and IT Consulting
Dover, DE 101 followers
IT & Subject Matter Consulting Expertise for Pharma, Life-sciences
About us
Pharmatek provides Onsite consulting / Strategic Staff Aug services to Pharma & Life-sciences, Medical Devices Industry. Our Consultants comes with strong IT expertise combined with deep understanding of various domain areas such as Pharma R&D , Validation & Compliance, Pharmacovigilance, Drug-safety, ECM, CRM, Clinical Trials , Enterprise Quality Systems, Lab Informatics, Manufacturing & Automation etc
- Website
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www.consultpharmatek.com
External link for Pharmatek
- Industry
- IT Services and IT Consulting
- Company size
- 11-50 employees
- Headquarters
- Dover, DE
- Type
- Privately Held
- Specialties
- Pharma, Biotech, Medical Devices, Information Technology, and Software
Locations
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Primary
Dover, DE, US
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Chennai, IN
Employees at Pharmatek
Updates
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Sushmita is hiring for Senior CQV Engineer at Austin, TX
Hello Connections! Pharmatek is actively hiring for Senior CQV Engineer at Austin, TX. What You’ll Do You will be responsible for performing quality oversight & approval of validations, change controls, records, & projects to ensure consistent deliver of high quality documents, processes, products, and processes. MAIN PURPOSE OF ROLE This position is responsible for providing quality support and oversight on product, process, and equipment related changes and implementations (validation & change control). QUALIFICATIONS Education Level Major/Field of Study OR Education Level Bachelor's Degree in Engineering or Technical Field or an equivalent combination of education and work experience EXPERIENCE Minimum 5 years experience in medical device/pharmaceutical manufacturing Process Validation experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971. Interested candidates apply here: https://lnkd.in/gh-vv7Ps hashtag #CQV hashtag #medicaldevice hashtag #pharmaceutical hashtag #manufacturing
Pharmatek Consulting Inc - Senior CQV Engineer in Austin
consultpharmatek.zohorecruit.in
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Hello Connections! Pharmatek is actively hiring for CQV – Lab Equipment Qualification Engineer at Indianapolis, IN. Responsibilities: Lead a Team through the qualification effort of making a lab and its equipment compliant to regulations and company procedures • Manage the validation and documentation related to complex computer systems, multiple pieces of equipment/large upgrades/extensive product updates • Perform functions of validation engineer – draft Validation Plans, Requirements, Test Cases, Summary Reports • Manage the systems and processes for change control and coordinate evaluation of proposed changes on laboratory equipment. • Change management process owner for validation involving new or modified equipment, processes, procedures, and products. In this role, validation engineers design and perform validation around lab equipment and computer systems. • Determine and delegate tasks amongst a team to complete assignment. • Conduct impact analysis for validation and change management • Coordinate teams to complete validation testing activities • Manage complete document management and approval through client’s process • Conducts regulatory impact analysis/assessment and, where warranted, makes recommendations. • Act as the Subject Matter Expert on various pieces of lab equipment Requirements • A minimum of a Bachelor’s degree in an Engineering or Scientific degree and five to ten years industry experience. Preferred: • 7+ years’ experience in GMP regulated environment (with Internship or co-op work experience considered as part of that experience) • Direct experience authoring/editing/executing validation documents for laboratory equipment (Cat. A, B &C) • Expert knowledge of FDA regulations, ISPE guidelines and ISO standards including: • Good Documentation Practice (GDP) in the pharmaceutical environment • 21 CFR Part 11 Interested candidates apply here: https://lnkd.in/deuY2nFf #CQV #medicaldevice #pharmaceutical #manufacturing
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Sushmita is hiring for Senior CQV Engineer at Austin, TX. Interested candidates apply: https://lnkd.in/gK4Ct4PW
Hello Connections! Pharmatek is actively hiring for Senior CQV Engineer at Austin, TX. What You’ll Do You will be responsible for performing quality oversight & approval of validations, change controls, records, & projects to ensure consistent deliver of high quality documents, processes, products, and processes. MAIN PURPOSE OF ROLE This position is responsible for providing quality support and oversight on product, process, and equipment related changes and implementations (validation & change control). QUALIFICATIONS Education Level Major/Field of Study OR Education Level Bachelor's Degree in Engineering or Technical Field or an equivalent combination of education and work experience EXPERIENCE Minimum 5 years experience in medical device/pharmaceutical manufacturing Process Validation experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP, ISO 13485, and ISO 14971. Interested candidates apply here: https://lnkd.in/gh-vv7Ps #CQV #medicaldevice #pharmaceutical #manufacturing
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Sushmita is hiring for CSV SME at College Station, Texas. https://lnkd.in/gmckZuYQ
Hello Connections! Pharmatek is actively hiring for Computer Systems Validation (CSV) - SME. CSV SME to act as a reviewer for validation protocols (to include Data Integrity and periodic review) and documentation to ensure protocol accuracy essentially acting as a QAV resource. Experience with the following platforms: DeltaV, Unicorn, BMRAM, MODA, standalone skids, etc. Interested candidates apply here: https://lnkd.in/gbaHc7MA #SME #CSV #texas #opentowork #hiring
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Sushmita is hiring for Construction Safety Program Manager. Interested candidates apply here: https://lnkd.in/g-pFMitw
Hello Connections! Pharmatek is actively hiring for Construction Safety Program Manager. Candidates with working experience in Pharmaceutical, Medical device, Life sciences and Manufacturing environments such as GMP, cGMP are accepted. Mainly looking for Construction and Safety manager Location: Onsite at Ohio Contract – 6 months Interested candidates apply here: https://lnkd.in/gDWPFi-D #construction #safety #manager #unitedstatesjob #ohiojobs #opentowork #hiring
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Hello Connections! Sushmita V is Hiring for Lead Quality/GxP Auditor. If interested, Connect at [email protected] #hiring #opentowork #northcarolina #openrole #gxp #gmp #audit
Hello LinkedIn Connection! Pharmatek is Hiring for Lead Quality/GxP Auditor at Cincinnati, OH. Providing employment benefits and stability in otherwise turbulent times. Excellent role with earning potential! Requirements: ➡️ Minimum 3 years of GxP auditing experience in related industry ➡️ Minimum of 5 years of experience within Pharmaceutical / Biotech / Medical Device industry ➡️ Experience working in a GxP (regulated) environment. ➡️ Experience in technical writing ➡️ B.S./B.A. in scientific discipline as a minimum Please share me your CV at: ➡️ [email protected] Apply for the job here: https://lnkd.in/gJtBQar5 *NOTE: Applicants must be eligible to work full-time in the United States with a valid work Visa.* #urgentrequirement #hiring #opentowork #Pharmaclient #audit #gxp Raghu Rajagopal
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Pharmatek reposted this
Hello LinkedIn Connection! Pharmatek is Hiring for Senior Project Engineer at Cincinnati, OH. This is an excellent opportunity to get into an industry that is booming! Providing employment benefits and stability in otherwise turbulent times. Excellent full time role with earning potential! Requirements: ➡️ Experience in Packaging LINES ➡️ Experience with Fillers Labelizers, Case Packaging, Palletizers Installation, Start up and Validation experience ➡️ Write and execute protocols ➡️ Engineering tracking ➡️ Serialization Experience- System used (Antares) preferred if they have this but not mandatory Please share me your CV at: ➡️ [email protected] *NOTE: Applicants must be eligible to work full-time in the United States with a valid work Visa. Not for Candidates without a work visa valid to the US or located in other countries.* #urgentrequirement #hiring #opentowork #Pharmaclient #packaging #jobsearch #cfbr #ohiojobs
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Hello LinkedIn Connection! Pharmatek is Hiring for Senior Project Engineer at Cincinnati, OH. This is an excellent opportunity to get into an industry that is booming! Providing employment benefits and stability in otherwise turbulent times. Excellent full time role with earning potential! Requirements: ➡️ Experience in Packaging LINES ➡️ Experience with Fillers Labelizers, Case Packaging, Palletizers Installation, Start up and Validation experience ➡️ Write and execute protocols ➡️ Engineering tracking ➡️ Serialization Experience- System used (Antares) preferred if they have this but not mandatory Please share me your CV at: ➡️ [email protected] *NOTE: Applicants must be eligible to work full-time in the United States with a valid work Visa. Not for Candidates without a work visa valid to the US or located in other countries.* #urgentrequirement #hiring #opentowork #Pharmaclient #packaging #jobsearch #cfbr #ohiojobs
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