
Sr Associate Qc
2 days ago
Career Category Quality Sr Associate QC - QC Systems Templating Role Name Sr Associate QC Department Name Quality Control Role GCF 4 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases and make people s lives easier fuller and longer We discover develop manufacture and deliver innovative medicines to help millions of patients Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation using technology and human genetic data to push beyond what s known today ABOUT THE ROLE Role Description Let s change the world Amgen is hiring for a Senior Associate to support the Electronic Lab Notebook ELN and consumable inventory system infrastructure in the Quality Control QC network This candidate will primarily work a shift-based schedule to enable the business in delivering Amgen s mission to serve patients The candidate may need to work outside of his her routine workday to support business needs The individual will be required to work from our office located in Hyderabad India Amgen India-AIN and provide remote support from AIN to Amgen sites across multiple time zones globally Roles Responsibilities This position will be responsible for creating revising peer-reviewing and qualifying templates for analytical method executions in ELN which includes ELN interfaces with other systems such as LIMS Empower and Chromeleon Creation and revision of consumable templates and supplementary master data will also be in the scope of responsibility In addition this position will collaborate with the US-based Master Data Group MDG and will also be involved in ELN template administration registration activities ensuring tasks align with procedures best practices and service level agreements for QC standardization Coordination with site representatives and other ELN template builders and qualifiers is required to convert QC source documents into ELN templates accurately Coordination with members within the team at AIN on the same shift and members of the team at AIN on different shifts will be critical in ensuring deliverables are met in accordance with schedule To effectively provide support candidates must demonstrate proficiency in virtual communication tools and have experience managing remote collaborations Secondary responsibilities may include cross-training into LIMS Empower and Chromeleon The following are some examples of tasks for the position Creation and revision of ELN templates Peer reviewing templates built by colleagues Qualification of ELN templates Creation and revision of consumable templates Collaboration with method subject matter experts template builders and template qualifiers throughout the QC network Ensuring training is up to date Additional responsibilities may involve Providing performance metrics Driving global QC system alignment Understanding prioritization of requests with the QC network Basic Qualifications and Experience Any degree with 5-8 years of Pharma and Biotech commercial or clinical manufacturing Quality Control experience Functional Skills QC lab testing experience Proficiency in ELN applications Knowledge of Data Integrity Requirements for QC systems Microsoft Office proficiency Familiarity with Good Manufacturing Practices Soft Skills Excellent English verbal and written communication skills Problem-solving and troubleshooting abilities Independence in delivering right first time EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race color religion sex sexual orientation gender identity national origin protected veteran status or disability status We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process to perform essential job functions and to receive other benefits and privileges of employment Please contact us to request an accommodation
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Associate Qc
2 weeks ago
Hyderabad, Telangana, India Amgen Full time**India - Hyderabad** **JOB ID**: R-221324 **ADDITIONAL LOCATIONS**: - India - Hyderabad **WORK LOCATION TYPE**: On Site **DATE POSTED**: Jul. 25, 2025 **CATEGORY**: Quality **Associate QC** - QC Systems Templating** **Role Name**:Associate QC **Department Name**:Quality Control **Role GCF: 3** ABOUT AMGEN Amgen harnesses the best of biology and...
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Associate QC
2 weeks ago
Hyderabad, India Amgen Full timeAssociate QC – QC Systems Templating Role Name: Associate QC Department Name: Quality Control Role GCF: 3 ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world's toughest diseases, and make people's lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients....
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Regulatory Affairs Sr Associate
2 weeks ago
Hyderabad, Telangana, India Amgen Full timeCareer Category Regulatory The Senior Associate in Regulatory Affairs at Amgen plays an important role in ensuring that the company s products meet and maintain regulatory standards They assist in preparing submissions for regulatory agencies keep updated on changes in regulatory legislation and guide various teams within the company to ensure...
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Regulatory Affairs Sr Associate
2 weeks ago
Hyderabad, India Amgen Full timeThe Senior Associate in Regulatory Affairs at Amgen plays an important role in ensuring that the company's products meet and maintain regulatory standards. They assist in preparing submissions for regulatory agencies, keep updated on changes in regulatory legislation, and guide various teams within the company to ensure compliance with applicable...
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Sr Manager
2 weeks ago
Hyderabad, India Curateq Biologics Full timeRole & responsibilities Suggested position: Sr Manager / Manager Education: Post Graduation (Life sciences preferred) Total Exp: 15-17 Years (Biopharma is preferred) Others: Ready to support in different shifts Responsibilities: Mainly responsible to review of Harvest, Drug Substance and Drug Product analytical (Biosimilars) raw data and analytical trends...
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Walk Ins- QC
2 weeks ago
Hyderabad, India MSN Group Full timeGreetings from MSN Laboratories... We are conducting a walk-in interview for Experienced & Freshers candidates in Our APICHEM Unit Vangapalli (Near to Yadagirigutta) on 5th Sept 2025 (Friday). Department- Production Req Exp-3 to 8 Yrs Qualification- B. Sc Chemistry/ Any Graduate Designations- Executive/ Jr. Executive/ Sr. Executive Department- QCReq...
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Walk Ins- QC
2 days ago
Hyderabad, Telangana, India MSN Group Full time ₹ 6,00,000 - ₹ 12,00,000 per yearGreetings from MSN Laboratories...We are conducting a walk-in interview for Experienced & Freshers candidates in Our APICHEM Unit Vangapalli (Near to Yadagirigutta) on 5th Sept 2025 (Friday).Department- ProductionReq Exp-3 to 8 YrsQualification- B. Sc Chemistry/ Any GraduateDesignations- Executive/ Jr. Executive/ Sr. ExecutiveDepartment- QCReq...
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Regulatory Compliance Change Assessor
4 weeks ago
Hyderabad, Telangana, India Amgen Inc Full timeJob DescriptionRoles & Responsibilities:Key responsibilities of the Regulatory Sr Associate include:- Reviews change records to evaluate impact of the change with respect to reportability and product restrictions for any product in scope.- Defines and documents the reporting and product distribution restriction requirements for the change within the change...
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Prod Compliance Associate Sr
7 days ago
Hyderabad, Telangana, India Amazon Full time ₹ 5,00,000 - ₹ 12,00,000 per year"Please note that this job is a seasonal role (FTC) for 12 months on the payroll of Amazon."Job Description is looking for a smart, enthusiastic, hard-working, and creative candidate to join the Brand Protection Business Operations team as a Prod Compliance Associate Sr. This position offers an exciting introduction to the Amazon Marketplace and provides a...
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Tmf Compliance Associate
7 days ago
Hyderabad, Telangana, India Novartis Full time392251BR **TMF Compliance Associate**: India **About the role** Your responsibilities include, but are not limited to: - Support QC/completeness checks on all global TCO study TMFs in accordance with Novartis SOPs, working practices and ICH/GCP Guidelines. Follow-up with the CTT to resolve quality issues identified and escalate potential SOP/WP...