📋 Job Details at a Glance 📍 Location Goa, India 🏢 Company Teva 👥 Experience 8-10 years 🎓 Qualification B.Pharm / M.Pharm / M.Sc 📅 Eligible Batch 2023, 2024, 2025, 2026 📄 Job Type Full Time 💰 Salary Not Disclosed 🏢 Industry Non-Tech 🛠 Key Skills Quality Analysis Laboratory Processes Calibration Documentation Reporting Quality Control Analyst I at Teva — Full Details & How to Apply Teva is seeking a Quality Control Analyst I in Goa, India , to ensure the highest quality standards in pharmaceutical products. This role is crucial for maintaining Teva's commitment to excellence in healthcare, offering a unique chance to contribute to the safety and efficacy of vital medications. As a pivotal position in the pharmaceutical industry, this role not only promises professional growth but also the opportunity to make a significant impact on public health. In today's fast-evolving pharmaceutical landscape, the role of a Quality Control Analyst I has never been more critical. With increasing regulatory scrutiny and a heightened focus on product safety, professionals in this field are essential for ensuring compliance with stringent quality standards. The demand for skilled analysts is on the rise, making this an opportune time to enter the field. As a Quality Control Analyst I , you will play a vital role in upholding the integrity of pharmaceutical products, a responsibility that is both challenging and rewarding. Teva stands out as an employer in the pharmaceutical sector due to its global reach and commitment to innovation. With a reputation for fostering a culture of excellence, Teva provides its employees with the tools and resources necessary for professional development. The company’s emphasis on quality and compliance not only enhances its product offerings but also cultivates a work environment that encourages continuous learning and growth. Joining Teva means being part of a team that is dedicated to making a difference in healthcare. This role is ideal for both freshers and candidates with up to 10 years of experience . Candidates must hold a B.Pharm, M.Pharm, or M.Sc degree and be from the eligible batches: 2023, 2024, 2025, and 2026 . If you possess a passion for quality analysis and laboratory processes, this position offers a pathway to develop specialized skills in a reputable company. As a Quality Control Analyst I , you will gain invaluable experience in quality analysis , laboratory processes , and calibration . You will also enhance your skills in documentation and reporting , which are critical for ensuring compliance with industry regulations. This role will equip you with the expertise needed to excel in quality control, making you a sought-after professional in the pharmaceutical industry. NexisGrow.com features this opportunity as part of its curated non-tech job listings. All details are sourced from the official job posting, ensuring you have the most accurate and up-to-date information to apply online for this Quality Control Analyst I position at Teva . Job Role & Responsibilities The role of a Quality Control Analyst I at Teva is pivotal in ensuring that both raw materials and finished products meet stringent quality standards. This position plays a crucial part in maintaining the integrity of pharmaceutical products, thereby safeguarding consumer health and compliance with regulatory requirements. Conduct quality analysis of raw materials and finished products to ensure compliance with both internal and external standards, thereby ensuring product safety and efficacy. Utilize laboratory equipment and software for calibration and testing, ensuring accurate and reliable results that meet industry benchmarks. Collaborate with cross-functional teams , including R&D and production, to address quality issues and implement corrective actions effectively. Analyze data and generate reports on quality metrics, providing insights for continuous improvement initiatives that enhance operational efficiency. Take ownership of quality documentation processes, ensuring all records are maintained accurately and in compliance with regulatory standards. Prepare and present findings in quality meetings , effectively communicating issues and solutions to stakeholders to foster a culture of transparency. Identify opportunities for innovation in quality control processes , contributing to the overall efficiency of laboratory operations. Participate in internal audits and inspections, ensuring that all quality processes adhere to regulatory requirements and industry best practices. This role embodies an ownership culture, where the Quality Control Analyst I is empowered to make impactful decisions that drive quality improvements and enhance the overall performance of Teva . Required Skills & Technical Competencies The ideal candidate for the Quality Control Analyst I role at Teva must possess a robust skill profile that combines technical expertise with analytical capabilities. This blend is essential for ensuring product quality and compliance in a highly regulated environment. Technical Skills Quality Analysis — critical for ensuring product safety and efficacy, directly impacting consumer health. Laboratory Processes — hands-on experience in laboratory settings is essential for executing quality tests effectively. Calibration — proficiency in using calibration tools and software enhances the accuracy of quality assessments. Documentation — advanced proficiency in documentation practices is expected to maintain compliance with industry regulations. Reporting — ability to analyze data and generate comprehensive reports on quality metrics for stakeholders. Data Analysis — strong analytical skills necessary to identify trends and address quality issues promptly. Soft Skills & Professional Competencies Problem-solving — adept at identifying issues and developing effective solutions in a timely manner. Communication skills — must effectively convey complex information to various stakeholders. Attention to Detail — essential for maintaining high standards in quality documentation and analysis. Team Collaboration — ability to work seamlessly with cross-functional teams to achieve common goals. Good to Have (Bonus) Certifications in Quality Control — such as Six Sigma or ISO standards, can enhance an application. Experience with Laboratory Management Software — familiarity with tools that streamline laboratory processes. Knowledge of Regulatory Compliance — understanding of FDA or EMA guidelines is advantageous. To effectively showcase these skills in a resume or interview for the Quality Control Analyst I role, candidates should provide specific examples of past experiences that demonstrate their proficiency in quality analysis , laboratory processes , and problem-solving capabilities. Eligibility Criteria This role is designed for candidates who are passionate about quality assurance in the pharmaceutical industry and possess the necessary educational background and experience. Ideal applicants will have a blend of academic credentials and practical experience. Candidates must hold a B.Pharm, M.Pharm, or M.Sc degree, ensuring a solid foundation in pharmaceutical sciences. Eligible batches include 2023, 2024, 2025, and 2026 graduates, targeting recent graduates and those with relevant experience. A minimum of 8-10 years of experience in quality control or related fields is preferred. A minimum CGPA of 6.0 is recommended to demonstrate academic proficiency in relevant subjects. Prior experience in a laboratory setting is essential for executing quality tests effectively. Certifications in quality control or laboratory management can enhance an application, showcasing a commitment to professional development. Documentation & Portfolio Requirements Applicants should prepare a well-structured resume highlighting relevant experiences and skills. Including any certifications in quality control or laboratory management will strengthen the application. A portfolio showcasing past projects or case studies related to quality analysis can also be beneficial. Pro Tip: Tailor your resume to emphasize your experience in quality analysis and laboratory processes , as these are critical for the Quality Control Analyst I role at Teva . Salary & Benefits 💰 Compensation Not Disclosed The compensation philosophy at Teva emphasizes providing a competitive salary that aligns with industry standards, particularly in the pharmaceutical sector. While specific salary details for the role of Quality Control Analyst I are not disclosed , candidates can expect a robust compensation package that reflects their skills and experience. What Your CTC Could Include Health Insurance — comprehensive coverage for employee and family worth ₹5 lakh annually Retirement Benefits — contributions to provident fund and gratuity schemes Performance Bonuses — annual bonuses based on individual and company performance Paid Time Off — generous vacation and sick leave policies Flexible Work Hours — options for hybrid work to promote work-life balance Additional Perks & Benefits Annual Learning Budget — up to ₹25,000 per year for certifications, courses, and conferences Meal Allowances — daily meal support to enhance employee satisfaction Transportation Support — assistance with commuting costs Employee Assistance Programs — mental health and wellness resources Team-building Activities — regular events to foster a collaborative work environment Career Progression & Salary Growth At Teva , career progression is a priority, with clear promotion timelines and an internal promotion policy that encourages growth. Employees can expect annual performance reviews that typically result in salary raises of 5-10% , depending on individual contributions and company performance. NexisGrow.com tip: When discussing salary, emphasize your relevant experience and the value you bring to Teva to negotiate effectively. Selection Process The hiring philosophy at Teva focuses on finding candidates who not only possess the necessary technical skills but also align with the company's values and culture. The selection process for the Quality Control Analyst I role is designed to thoroughly evaluate both qualifications and fit. 1 Round 1: Initial Screening — online application review to assess qualifications and fit for the role. 2 Round 2: Technical Interview — focused on quality control principles and laboratory processes to evaluate expertise. 3 Round 3: Final Interview — discussion with HR and team leaders to assess cultural fit and alignment with company values. 4 Final Offer Stage — includes background checks and reference verification to ensure candidate suitability. What Each Round Tests Round 1 evaluates your educational background and relevant experience . Round 2 assesses your technical knowledge in quality control and laboratory processes. Round 3 focuses on your communication skills and how well you align with the Teva culture. Timeline & Expectations The entire process from application to offer typically takes 4-6 weeks , depending on candidate availability. Expect timely communication from Teva regarding your application status and next steps. Interview Prep Tip: Familiarize yourself with Teva's core values and be ready to discuss how your experiences align with their mission. How to Apply for Quality Control Analyst I at Teva Apply Now — Teva Create Your Profile — visit the application portal and set up your profile. Resume Submission — upload your resume, highlighting relevant experience in quality control and laboratory processes. Fill Out the Application Form — ensure all fields are completed accurately. Track Your Application — monitor your application status through the portal. Prepare for Interviews — review potential interview questions and align your experiences with the role. Resume & Profile Tips for This Role Highlight Relevant Experience — focus on your background in quality control and laboratory techniques. Showcase Certifications — include any relevant certifications or training in quality assurance . Emphasize Soft Skills — particularly problem-solving and communication skills . Detail Technical Skills — mention any experience with laboratory equipment and processes. Note: Applications are reviewed on a rolling basis, so early submission is encouraged to increase your chances. Apply Now — Official Link NexisGrow.com does not charge any fees for job applications. Frequently Asked Questions Interview · Role · Salary · Growth ? What are the eligibility criteria for the Quality Control Analyst I role at Teva? Eligibility Tap to expand + Answer Candidates must hold a B.Pharm, M.Pharm, or M.Sc degree, with eligibility for batches 2023-2026. Experience of 8-10 years is preferred. ? What is the interview process for Quality Control Analyst I at Teva? Interview Tap to expand + Answer The interview process includes an online application review, a technical interview on quality control principles, and a final HR interview. ? What skills and tools will I need for this role? Skills Tap to expand + Answer Key skills include quality analysis, laboratory processes, and advanced documentation practices, with proficiency in calibration tools being advantageous. ? What is the salary and compensation for this role? Salary Tap to expand + Answer Salary details are not disclosed, but Teva offers competitive compensation and performance-based bonuses. ? Is this role work from home, hybrid, or onsite? Work Mode Tap to expand + Answer This role is primarily onsite in Goa, aligning with industry norms for quality control positions. ? What is the career growth path after joining Teva as a Quality Control Analyst I? Growth Tap to expand + Answer Career growth includes opportunities for promotions within 1-2 years, with potential for lateral moves into other departments. ? How should I prepare for the Quality Control Analyst I interview at Teva? Preparation Tap to expand + Answer Focus on understanding quality control processes, laboratory techniques, and prepare to discuss your relevant experience in detail. ? How do I apply and what documents are needed? Application Tap to expand + Answer Apply through the official link, ensuring your resume highlights relevant experience and skills specific to quality control. ? Is there a probation period and what does it involve? Probation Tap to expand + Answer Typically, there is a 3-6 month probation period focused on performance evaluation and integration into the team. ? What is the work culture like at Teva? Culture Tap to expand + Answer Teva promotes a culture of collaboration, diversity, and continuous learning, fostering a supportive environment for all employees. Ready to Apply? Don't Miss This Opportunity! Apply only via the official link. NexisGrow.com charges zero application fees. 👉 Apply Now — Official Link NexisGrow.com does not charge any application or registration fees. Beware of fraudulent offers. Naukri ki baat, NexisGrow ke saath • NexisGrow.com