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Quality Services Specialist - MTL (Bengaluru, KA, IN, 560034) @ Aceto US LLC

Bengaluru, KA, IN, 560034OnsiteFull-time
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About this role

<p><span style="font-size:12.0pt"><span><span style="font-size:11.0pt"><span>Actylis is a global solutions provider with over 75 years of experience, specializing in streamlining the management of critical ingredients and raw materials for our business partners.</span></span></span></span></p> <p> </p> <p><span style="font-size:12.0pt"><span><span style="font-size:11.0pt"><span>We offer both sourcing and manufacturing solutions tailored to meet diverse and evolving needs, ensuring a reliable, agile, and secure supply network. Our commitment to customization allows us to create flexible solutions, whether it’s a unique specification, custom packaging, or tailored logistics strategies.</span></span></span></span></p> <p> </p> <p><span style="font-size:12.0pt"><span><span style="font-size:11.0pt"><span>With deep expertise in quality and regulatory compliance, sourcing and logistics management, analytical services, and R&amp;D support, we reduce complexities and mitigate risks, empowering our partners to focus on growing their business.</span></span></span></span></p> <p> </p> <p><span style="font-size:12.0pt"><span><span style="font-size:11.0pt"><span>In furtherance of that goal, Actylis is seeking new members of the team. This expansion, coupled with a comprehensive benefits package, and opportunities for challenge and growth, make Actylis the ideal place to work and thrive. We hope you’ll consider joining us!</span></span></span></span></p> <p style="text-align:justify"> </p> <p><strong>Position summary: </strong><br>The Quality Service Specialist primarily supports commercial and customer quality document requests.</p> <p> </p> <p><strong>Key Responsibilities:</strong></p> <p> </p> <p><strong>Develop Goals and Motivations for Excellence in Quality Support Services:</strong></p> <ul> <li>Place the interests of the Commercial Team and the Customer first; our success depends on their success.</li> <li>Be highly responsive and timely to the Commercial Team and Customer Key Accounts.</li> <li>Meet deadlines; communicate status and delays to the Team and customers proactively.</li> <li>Pursue an unrelenting quest for quality; use speed and simplicity to achieve goals.</li> <li>Communicate pleasantly and effectively.</li> <li>Demonstrate professional etiquette and courtesy when interfacing with customers.</li> <li>Conduct oneself with the highest level of integrity and business ethics.</li> <li>Commit to teamwork; seek out and use the ideas and skills of all colleagues.</li> <li>Reach for the highest standards of performance; show a passion for winning.</li> </ul> <p> </p> <p><strong>Commercial Team Support Function:</strong></p> <p> </p> <ul> <li><strong> Curate any and all Commercial Team, and direct Customer Requests</strong><br>- Process information received from Commercial Team personnel<br>- Manage and prioritize information to ensure timely delivery<br>- Organize and maintain documentation received and conduct follow-up as applicable<br>- Liaise with QA/QC and Technical department to resolve customer requests<br>- Complies with and adheres to all regulatory compliance areas, policies and procedures.<br>- Identifies and implements “best practices” in Quality Services.<br>- Performs other duties as assigned by Commercial Team in a proactive manner</li> </ul> <p> </p> <p><strong>Manage and Maintain Pertinent Logs (QA Document and Technical):</strong></p> <ul> <li>Keep the QA document and Technical logs updated</li> <li>Acknowledge requests within 48h if they are not completed</li> <li>Provide high-level summary of log status to the Senior Quality and Regulatory Manager and/or the Director semi-monthly</li> <li>Review weekly tasks and responsibilities with the Senior Quality and Regulatory Manager</li> </ul> <p> </p> <p style="text-align:left"><strong>Customer CDA/QAA – Commercial Team Requests</strong><br>• Initial review, propose revisions, follow up, signature coordination, and completion of customer confidentiality agreements (CDA), customer quality assurance agreements (QAA) and any quality-related agreements (e.g. Quality Technical Agreements (QTA), Customer Commitment Letter (CSL), etc.)<br>• Support the maintenance of the CDA and QAA log<br>- Customer Questionnaires<br>- A&amp;C Standard Quality System Overview<br>- SOP Document Master List<br>- Organizational Chart<br>- General Policy Statements<br><strong>• Customer Specific Questionnaires: provided to Key Customers</strong><br>- Initial review<br>- Finalize, signature collection<br>- Provide to Commercial Team, Customer Services, or directly to Customer<br><strong>• Product Regulatory Document Requests:</strong><br>- Residual Solvents statements (RS)<br>- BSE/TSE, GMO, and Allergen product compliance statements<br>- Allergen statements<br>- Melamine statements<br>- Metal Residues statements<br>- No Animal testing statements<br>- Other statements, e.g. Proposition 65 GRAS status, suitability etc.<br><strong>• Respond to Product Information Requests</strong><br>- Specifications<br>- Typical COA<br>- Certificate of Origin<br>- Test Methods<br>- Shelf Life Letter<br>- Manufacturer and Supply Chain Information<br>- Packaging Specification/Information<br>- Storage Conditions Statement<br>- Stability Statement, Stability Data<br>- Example Label (Mater Label)<br>- Other product information statement (e.g. supply chain, manufacturing flow chart (MFC), etc.)</p> <p> </p> <p><strong>Document Delivery System Design, Implementation and Maintenance</strong><br>• Manage Excipient Information Packages based on IPEC guidelines<br>• Manage the maintenance of Document Dossiers for A&amp;C’s push products<br>• Assist in the design and implementation of Web-based Specification, COA and SDS self-serve document access<br>• Suggest other document types suitable for Web-based self-serve document access</p> <p> </p> <p><br><strong>External Audits Support</strong> <br>• Act as liaison in organizing the timing and set-up of customer audits </p> <p> </p> <p> </p> <p><strong>Customer Requirements Initial Review </strong><br>• Initial review of customer requirements against: <br>• Existing A&amp;C products specifications <br>• Proposed source materials specifications <br>• New source materials specifications </p> <p> </p> <p><strong>Ancillary tasks/Responsibilities:</strong><br>Support to the global team when required, ensuring flexibility for special assignments.</p> <p> </p> <p><strong>Qualifications &amp; Experience:</strong></p> <p>Bachelor’s degree in science (Chemistry)or related field.</p> <p>Minimum of 3 - 6 years of experience in Pharma industry.</p> <p>Quality Systems Knowledge (ISO and GMP) 3 years experience.<br>Member of the Order of Chemists.<br>Industry knowledge.</p> <p> </p> <p><strong>Functional/Technical Competencies &amp; Skillsets</strong></p> <p><strong> </strong></p> <ul> <li>Quality Systems knowledge (ISO and GMP).</li> <li>Proficiency in quality management systems and auditing techniques.</li> <li>Strong analytical and problem-solving skills.</li> <li>Excellent communication and interpersonal skills.</li> <li>Ability to read, understand and apply complex instructions/regulations.</li> <li>Ability to work independently and as part of a team.</li> <li>Attention to detail.</li> <li>Self-starter.</li> </ul> <p> </p> <p><strong>SUPERVISORY RESPONSIBILITIES: </strong>N/A</p> <p> </p> <p> </p><p>Actylis is an Equal Opportunity Employer. Actylis does not discriminate on the basis of race, religion, color, sex, gender identity or expression, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided based on qualifications, merit, and business need..</p>

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