WALK IN TEST FOR THE SELECTION OF TECHNICAL ANALYST – CHEMISTRY ON CONTRACT BASIS FOR ENGAGING AT QUALITY EVALUATION LABORATORY, SPICES BOARD

 

WALK IN TEST FOR THE SELECTION OF TECHNICAL ANALYST – CHEMISTRY ON CONTRACT BASIS FOR ENGAGING AT QUALITY EVALUATION LABORATORY, SPICES BOARD

Spices Board, invites application from the qualified candidates preferably residing in the regions/ Corporations/ Municipalities, where the Quality Evaluation Laboratory of the Board is situated , i.e. at Tuticorin for short contractual appointment of Technical Analyst (Chemistry) initially for a period of one year and may be further extendable by one more year as per the requirement and based on performance

Essential Qualification Chemistry - Post Graduate degree in Chemistry / Applied Chemistry/ Analytical Chemistry/ Organic Chemistry from a recognised University/ Institute

Date and Time for walk-in-test 03-02-2025 at 11 AM Candidates shall report at the venue one hour before the commencement of written test for verification of original certificates)

Venue for written test Spices Board ,Quality Evaluation Laboratory, World Trade Avenue, Near Seapol Logistics, VOC, Newport,Tuticorin,Tamilnadu-628004 Ph: 0461 – 2903011 Method of Selection: Selection will be through multiple choice (MCQ) written test of PG level standard for hour duration.

Eligible candidates may appear for a walk -in- test along with their applications in prescribed format (Annexure-I ), original certificates for proof of identity, age, education, experience and caste and one set of attested copies of the certificate (Proof for identity, age, education, experience and caste) on the date and time at the address given above

Candidates are advised to check Notifications/opportunities in Board’s website www.indianspices.com for updates and not to rely on information from 3rd party websites.

3. Before applying, candidates should ensure that they fulfil the eligibility criteria for the post.

4. Candidates are advised to keep their e-mail ID and mobile number active for receiving communication from the Spices Board.

5. In case it is detected at any stage of selection process that a candidate does not fulfil the eligibility norms and/or that he/she has furnished any incorrect/false information or has suppressed any material fact(s), his/her candidature will stand cancelled. If any of these shortcomings is/are detected even after appointment, his/her services are liable to be terminated.

 6. Decisions of Spices Board in all matters regarding eligibility, conduct of test, detailed test and selection procedure would be final and binding on all candidates. No representation or correspondence will be entertained by the Board in this regard.

7. Any legal proceedings in respect of any matter of claim or dispute arising out of this vacancy notification and/or an application, tests, etc., in response thereto can be instituted only in Kochi and courts at Kochi only shall have sole and exclusive jurisdiction to try any cause/dispute. 8. Canvassing in any form will be a disqualification.

9. The eligibility of applicants with respect to age, educational qualification, experience etc. will be determined as on the date of written test. 10. The period of experience in a discipline/area of work, wherever prescribed, only after the date of acquiring the essential qualification will be counted.

 11. Spices Board reserves the right to modify/alter/restrict/enlarge/cancel the recruitment process, if need so arises, without issuing any further notice or assigning any reasons therefore. The decision of Spices Board will be final and no appeal will be entertained against this issue.

12. All queries/issues regarding the notification are to be addressed to the Scientist C & QEL i/c, Spices Board only through e-mail: srilatha.cm@nic.in

13. The engagement of candidates will be purely on contractual basis and under no circumstances are linked to regular appointments and cannot be regularized at any stage. 14. The validity of rank list will be for two years only

FOR ADVERTISEMENT CLICK HERE 

 

SPICES BOARD (Ministry of Commerce & Industry, Govt. of India) Recruitment of WALK IN TEST FOR SELECTION OF TRAINEES IN QUALITY EVALUATION LABORATORY (QEL)

 

SPICES BOARD  (Ministry of Commerce & Industry, Govt. of India) Recruitment of WALK IN TEST FOR SELECTION OF TRAINEES IN QUALITY EVALUATION LABORATORY (QEL)  

Trainees Trainee Analyst (Chemistry) – 03 (Three) Nos. (A panel will be prepared for selection of trainees for future requirements.)

Qualification  Trainee Analyst (Chemistry) : Essential:-Bachelor of Science Degree with Chemistry as one of the subject (applicable for triple major system only) or Bachelor degree in Chemistry, from a recognized university/ Institute, or equivalent.

Venue, Date and time of Walk-in-test Venue: SPICES BOARD,WORLD TRADE AVENUE, NEAR SEAPOL LOGISITCS, VOC NEW PORT, TUTICORIN-628004, TAMIL NADU Tel. 0461 - 2903011 Trainee Analyst Chemistry Date : 10-02-2025 Time : 11.00 AM

Instructions to candidates:  Eligible candidate appearing for the test should fill-in and sign the form placed as Annexure I of this notice and bring along with all necessary documents given below:

passport size color photograph, o original certificates for:  Identity proof ( Voter card, Driving license etc.)  Proof of age  Proof of education and training  Caste Certificate o One set of attested photocopies of the above document stapled to the filled-in and signed Annexure

1.      The number of trainees indicated is provisional and may vary at the time of selection.

2.      The selection as Trainee in Spices Board is only training and under no circumstances is linked to regular appointments and cannot be regularized at any stage

 FOR NOTIFICATION CLIC HERE

 

 

Why Choose Medical Writing? Career Opportunities in Medical Writing: Flexibility: High Demand: Diverse Career Paths:

 

Why Choose Medical Writing? Career Opportunities in Medical Writing: Flexibility: High Demand: Diverse Career Paths

Career Opportunities in Medical Writing

Medical writing is a dynamic and rewarding career option for professionals with a background in pharmacy, life sciences, or healthcare. It involves creating scientific and medical content tailored for various audiences, such as healthcare professionals, regulatory authorities, or the general public. With the increasing demand for high-quality medical content, this field offers ample opportunities for growth and development.

Why Choose Medical Writing?

Medical writing combines scientific knowledge with excellent communication skills. It is ideal for individuals passionate about science, research, and writing. Professionals in this field play a critical role in translating complex scientific data into clear, concise, and accurate documents.

Key benefits of a career in medical writing include:

·         Flexibility: Many roles offer remote or freelance opportunities.

·         High Demand: The pharmaceutical and healthcare industries require skilled writers to produce regulatory, marketing, and educational content.

·         Diverse Career Paths: A wide range of writing specialties allows professionals to choose based on their interests and expertise.

Career Paths in Medical Writing

1.      Regulatory Medical Writing

·         Involves preparing documents required for regulatory submissions, such as clinical study reports, protocols, investigator brochures, and common technical documents (CTD).

·         Requires a thorough understanding of regulatory guidelines and clinical trial data.

2.      Scientific/Publication Writing

·         Focuses on creating manuscripts, review articles, posters, and abstracts for journals and scientific conferences.

·         Ideal for those interested in academic and evidence-based writing.

3.      Medical Marketing Writing

·         Involves creating promotional content, such as brochures, websites, and advertisements, for healthcare products and services.

·         Requires creativity and an understanding of marketing strategies.

4.      Educational Medical Writing

·         Includes developing training modules, e-learning content, and educational material for healthcare professionals or patients.

·         Helps bridge the knowledge gap between science and its practical application.

5.      Freelance Medical Writing

·         Offers flexibility and independence to work on diverse projects across various niches.

·         Requires self-discipline and networking skills.

Skills and Qualifications

To excel in medical writing, professionals need:

·         Strong command of the English language.

·         In-depth knowledge of medical and scientific concepts.

·         Familiarity with industry guidelines such as ICH-GCP and regulatory standards.

·         Proficiency in tools like MS Office, referencing software, and publication platforms.

·         Analytical thinking and attention to detail.

How to Start Your Career

1.      Educational Background: A degree in pharmacy, life sciences, or a related field is essential. Additional certifications in medical writing can enhance your skills.

2.      Networking: Join professional associations like the American Medical Writers Association (AMWA) or European Medical Writers Association (EMWA).

3.      Portfolio Development: Create sample work or volunteer for small projects to showcase your expertise.

Conclusion

Medical writing offers a fulfilling career for those who love science and communication. With opportunities in diverse areas, it provides a platform to grow professionally while contributing significantly to the healthcare industry. Whether you choose regulatory writing, publication writing, or marketing, medical writing is a field that blends creativity with technical expertise, ensuring a bright and promising career path.

 

What is Pharmacovigilance? Different Job Designations and Profiles in Pharmacovigilance and Drug Safety

 

What is Pharmacovigilance? Different Job Designations and Profiles in Pharmacovigilance and Drug Safety

 

Pharmacovigilance is the pharmacological science relating to the detection, assessment, understanding and prevention of adverse effects, particularly long term and short term side effects of medicines. In general, Pharmacovigilance is the science of collecting, monitoring, researching, assessing and evaluating information from healthcare providers and patients on the adverse effects of medications, biological products, herbalism and traditional medicines with a view to: identifying new information about hazards associated with medicines preventing harm to patients. Pharmacovigilance is particularly concerned with adverse drug reactions, or ADRs, which are officially described as: “A response to a drug which is noxious and unintended, and which occurs at doses normally use for the prophylaxis, diagnosis or therapy of disease, or for the modification of physiological function.

Different Job Designations and Profiles in Pharmacovigilance and Drug Safety

Job Designations:

1.      Pharmacovigilance Associate/Officer:

·         Responsible for case processing, data entry, and initial assessment of adverse event reports.

·         Ensures accurate and timely documentation of drug safety information.

2.      Drug Safety Specialist:

·         Manages and analyzes safety data.

·         Prepares safety reports and conducts risk assessments.

·         Coordinates with clinical and regulatory teams.

3.      Pharmacovigilance Scientist:

·         Conducts detailed analysis and interpretation of safety data.

·         Prepares regulatory submissions and safety update reports.

·         Develops risk management plans and safety strategies.

4.      Signal Detection Specialist:

·         Monitors and analyzes data to identify safety signals.

·         Investigates potential safety issues and trends.

·         Recommends risk mitigation actions.

5.      Pharmacovigilance Manager:

·         Oversees pharmacovigilance operations and teams.

·         Ensures compliance with regulatory requirements and company policies.

·         Manages adverse event reporting and safety data management.

6.      Drug Safety Manager:

·         Manages safety surveillance activities and safety databases.

·         Coordinates with cross-functional teams to address safety concerns.

·         Ensures regulatory compliance in safety reporting.

7.      Regulatory Affairs Specialist:

·         Prepares and submits safety reports to regulatory authorities.

·         Monitors regulatory changes and ensures compliance.

·         Liaises with regulatory agencies on safety-related issues.

8.      Medical Reviewer:

·         Conducts medical review of adverse event reports and safety data.

·         Provides clinical insights into safety assessments and risk evaluations.

·         Collaborates with medical and scientific teams.

9.      Safety Data Analyst:

·         Analyzes safety data using statistical and analytical tools.

·         Prepares safety reports and presentations.

·         Supports signal detection and risk management activities.

10.  Risk Management Specialist:

·         Develops and implements risk management plans.

·         Monitors risk mitigation strategies and their effectiveness.

·         Collaborates with regulatory and clinical teams on safety issues.

11.  Pharmacovigilance Compliance Specialist:

·         Ensures adherence to pharmacovigilance regulations and guidelines.

·         Conducts audits and inspections.

·         Implements corrective and preventive actions.

12.  Pharmacovigilance Quality Assurance (QA) Manager:

·         Oversees quality assurance activities in pharmacovigilance.

·         Ensures compliance with SOPs and regulatory requirements.

·         Conducts internal audits and supports external inspections.

13.  Medical Information Specialist:

·         Provides information on drug safety and pharmacovigilance to healthcare professionals and patients.

·         Responds to safety-related inquiries.

·         Supports pharmacovigilance activities with medical expertise.

14.  Global Safety Lead:

·         Oversees global safety surveillance and pharmacovigilance activities.

·         Develops global safety strategies and policies.

·         Ensures coordination and compliance across international markets.

These roles are essential for ensuring the safety and efficacy of pharmaceutical products, safeguarding public health, and complying with regulatory standards.

 Who hires Pharmacovigilance Professionals?

·         Pharmaceutical Companies:

·         Major pharmaceutical companies with extensive drug portfolios and global operations.

·         Small to medium-sized pharmaceutical firms focusing on specific therapeutic areas.

·         Biotechnology Companies:

·         Firms developing biologics, biosimilars, and innovative therapies.

·         Contract Research Organizations (CROs):

·         Companies providing outsourced clinical research and pharmacovigilance services to pharmaceutical and biotechnology firms.

·         Regulatory Agencies:

·         Government bodies responsible for drug safety and regulation, such as the FDA (U.S. Food and Drug Administration), EMA (European Medicines Agency), MHRA (Medicines and Healthcare products Regulatory Agency), and others worldwide.

·         Pharmacovigilance Service Providers:

·         Specialized companies offering pharmacovigilance and drug safety services, including case processing, signal detection, and regulatory reporting.

·         Hospitals and Healthcare Institutions:

·         Organizations that conduct clinical trials and require pharmacovigilance professionals to monitor and report adverse events.

·         Academic and Research Institutions:

·         Universities and research centers involved in clinical research and pharmacovigilance studies.

·         Consulting Firms:

·         Companies providing expert advice and support on pharmacovigilance, regulatory compliance, and risk management.

·         Health Technology Companies:

·         Firms developing pharmacovigilance software and tools for data collection, management, and analysis.

·         Non-Governmental Organizations (NGOs) and Public Health Organizations:

·         Organizations focusing on global health initiatives, drug safety, and pharmacovigilance in developing countries.

·         Insurance Companies:

·         Firms that require pharmacovigilance expertise for risk assessment and management in healthcare coverage.

Who Can Build a Career in Pharmacovigilance?

1.      Life Sciences Graduates:

·         Individuals with degrees in biology, biochemistry, microbiology, biotechnology, pharmacology, and related fields.

2.      Pharmacy Graduates:

·         Pharmacists and those with degrees in pharmaceutical sciences or clinical pharmacy.

3.      Medical Professionals:

·         Physicians, nurses, and other healthcare professionals with clinical experience who want to transition into drug safety roles.

4.      Chemistry Graduates:

·         Those with a background in chemistry, particularly medicinal chemistry, can contribute to drug safety and pharmacovigilance activities.

5.      Public Health Graduates:

·         Individuals with degrees in public health, especially those who have specialized in epidemiology or health policy.

6.      Healthcare and Clinical Research Professionals:

·         Clinical research associates (CRAs), clinical trial coordinators, and other clinical research staff interested in focusing on drug safety.

7.      Regulatory Affairs Professionals:

·         Those already working in regulatory affairs can expand their expertise to include pharmacovigilance.

8.      Data Analysts and Statisticians:

·         Professionals with skills in data analysis and biostatistics, crucial for analyzing and interpreting safety data.

9.      Quality Assurance Specialists:

·         Individuals experienced in quality assurance and compliance can transition into pharmacovigilance to ensure adherence to regulatory standards.

10.  Biomedical Engineers:

·         Those with a background in biomedical engineering, especially those interested in medical device safety and vigilance.

11.  Experienced Professionals in Related Fields:

·         Individuals from related fields like toxicology, healthcare management, or medical writing can transition into pharmacovigilance roles with additional training