? Result-oriented professional offering 30 years of experience in Analytical Labs -Quality Assurance & Control across Chemicals, Petrochemicals, Pesticides, Oils, Mines, Polymers, Pigments, Pharmaceutical, and Nutraceutical Industries.

QAQC Laboratory Manager QMS & LMS Auditor  

Opdateret 03. februar 2024
Min uddannelse
1990 - 1992

Cand.scient. i Kemi

Københavns Universitet

Uddannelsesområde: Kemi, Biotek & Materialer
Periode: juni 1990 - juni 1992
Min erhvervserfaring
2015 - nu

QA QC Lab Manager

Virksomhedsnavn skjult

? Result-oriented professional offering 30 years of experience in Analytical Labs -Quality Assurance & Control across Chemicals, Petrochemicals, Pesticides, Oils, Mines, Polymers, Pigments, Pharmaceutical, and Nutraceutical Industries
? Act as a link between Production and Customer relating to Analytical & Quality of material issues.
? To ensure that all legal / statutory requirements are being met by the company.
? To ensure adequate monitoring of Analytical parameters and Laboratory Chemicals related safety requirements
? To report and follow up on corrective actions in case of non-compliance.
? To comply with Quality control authorities’ directives: adequate reporting to the authorities, liaise with authorities relating to analytical & product inspectorate laboratory issues.
? Understanding customer needs and requirements to develop effective quality control processes.
? Devising and reviewing specifications for products and RM
? Ensure adherence to health and safety guidelines as well as legal obligations.
? Supervise staff and provide guidance and feedback.
? Setting requirements for raw material or intermediate products for suppliers and monitoring their compliance
? Oversee all product and RM to identify deviations from quality standards.
? Inspect final output and compare properties to requirements.
? Approve the right products or reject defectives.
? Ensure the compliances of Quality and Regulatory requirements of products supplied in line with customer.
? Timely response to customer complaints To respond timely for customer complaints by submitting CAPA reports
? Timely response to review, approve and respond timely to customer questionnaires and quality agreements.
? Effectiveness of documentation, change control, deviation control to review, approve and control all system SOPs, track the effectiveness of change control, deviations.
? Continual Improvement to facilitate the analysis of various Mfg and QC data and coordinate with stakeholders to simplify the processes basis the trend of performance.
? Vendor audits / development: to lead vendor audit, qualification and evaluation process in line with plan agreed with Sourcing.
? To act as Site’s representative Manager and deal with marketing and customers and coordinate to fulfil their requirements. To monitor and coordinate the customer complaints and their timely resolution.
? To be responsible for arranging purchase of Chemicals and other Stores items required for the Laboratory.
? To be responsible for all purchase of Laboratory chemicals, material & Lab wares, their storage and consumption at self and plant level.
? To be overall responsible for keeping the necessary records and issuing certificates of all the Sections of Analytical Laboratory.
? To be responsible for protecting confidential information and proprietary rights of the activities conducted in the Analytical Laboratory.
? Leveraged understanding of QMS-ISO9001/ISO14000, ISO17025, and GLP
? Proven skills in analysing & interpreting unique problems, with combination of training experience & logical thinking; application of QC tools and identified process bottlenecks & product deficiencies.
? Expertise in validating quality processes by establishing product specifications & quality attributes, measuring production, documenting evidence, determining operational and performance qualification, and writing & updating quality assurance procedures.
? Excellence in conducting inspection of materials as per management requirement to ensure stringent quality control; implemented stage-by-stage quality system to ensure adherence to technical specifications and quality standards.
? Impressive success in supporting improvement initiatives, utilizing various tools and implementing ISO & GLP norms and process improvement measures as well as own area aimed to ensure quality, safety, productivity, on time delivery and supporting internal customers.
? Track record of modifying processes & establishing SOPs, streamlining workflow and creating work environment to optimize resource & capacity utilization and enhance productivity & operational efficiencies.
Arbejdsområde: Produktion
Periode: juli 2015 - nu
Mine kompetencer
Evner
capa customer complaint gc hplc iso 14001/iso 45001 iso/iec 17025 internal auditor5 qaqc qms lead audiitor uvspectroscopy vendor qualification wet lab
Sprog på arbejdsniveau
english hindi marathi
Mine præferencer
Jobtype
Freelance Fuldtidsjob
Arbejdsområde
Forskning & Udvikling Medicinal & Sundhed Naturvidenskab Topledelse
Geografi
Fyn Storkøbenhavn Sydsjælland & Øer Sønderjylland Østsjælland
Lønønske
2.500 DKK / måned
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