Social network you want to login/join with:
Regulatory Compliance Associate (12 Month FTC), Cambridge
Client:
Abcam Location:
Cambridge, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
21e79a9c367f Job Views:
88 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Company Description For over 20 years, Abcam has been providing tools the scientific community needs to enable faster breakthroughs in critical areas like cancer, neurological disorders, infectious diseases, and metabolic disorders. We believe that to continue making progress, we need to work together in new ways. We need your own unique perspective as well as this of our people to make an always greater impact on the world. This community needs people like you: dedicated, agile and above all audacious so we can truly bring progress forward. Job Description This exciting role will support Abcam’s Regulatory Compliance Senior Specialist & Department Manager with the authoring and maintenance of product safety data sheets (SDS) and hazard data for inclusion on product labels in accordance with Global Harmonized System, REACH, and any other applicable global chemical regulations. This role will interface closely with Category and Supplier Management Teams and will principally involve SDS updates, authoring new SDS as required and answering queries from global colleagues and customers. Responsibilities Generate compliant SDS using Abcam’s dedicated SDS authoring application, WERCS Maintain existing product SDS ensuring any updates to hazards and/or legislation are implemented Support management of the team dedicated inbox, where we receive customer & internal SDS requests & compliance enquiries Carry out routine governance and oversight checks, particularly for antibody, protein, peptides & lysates portfolios Provide general Regulatory Compliance Team support You will have a strong knowledge in Excel & other MS Office applications. You will have experience working with large datasets. You will have excellent attention to detail and written and verbal communication skills to resolve internal & external product data queries in a timely manner. You will have the ability to prioritise and process large amounts of data in a logical and efficient manner, ensuring our customers receive accurate data. You will be a confident individual and be able to work independently. You will hold yourself and others to high standards of accuracy and attention to detail in a fast-paced environment. Familiarity with global chemical regulations (EU CLP (Classification, Labelling and Packaging), GHS, REACH) & experience in SDS authoring would be advantageous, but not essential due to basic training being provided, as would any other experience of a previous junior regulatory affairs or product compliance role. Knowledge of the SDS authoring application WERCS would be advantageous, as would any other experience with this type of application. Qualifications You will be educated to at least degree level (or equivalent), possess a knowledge of Chemistry, Life Science, or a related field. Additional Information We know that when it comes to benefits, no one size fits all. Flexibility and choice matter which is why, in addition to market competitive salaries, we offer you a flexible benefits package which is tailored to your unique needs and support your financial, physical and emotional wellbeing. This includes 18 weeks fully paid maternity leave, 6 weeks fully paid paternity leave as well as highly flexible working and much more. Besides, your development will be integral to your experience here. You will grow alongside other talented minds, in ways you may often find unexpected. When people come together, incredible things happen. Here you’ll work in a safe environment where you can be who you truly are. We’ll champion and celebrate your uniqueness throughout your journey with us. This is how we excel at partnering with the scientific community no matter the challenge, ultimately helping solve the world’s most critical diseases. Find out more about Diversity & Inclusion at Abcam.
#J-18808-Ljbffr
Client:
Abcam Location:
Cambridge, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
21e79a9c367f Job Views:
88 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
Company Description For over 20 years, Abcam has been providing tools the scientific community needs to enable faster breakthroughs in critical areas like cancer, neurological disorders, infectious diseases, and metabolic disorders. We believe that to continue making progress, we need to work together in new ways. We need your own unique perspective as well as this of our people to make an always greater impact on the world. This community needs people like you: dedicated, agile and above all audacious so we can truly bring progress forward. Job Description This exciting role will support Abcam’s Regulatory Compliance Senior Specialist & Department Manager with the authoring and maintenance of product safety data sheets (SDS) and hazard data for inclusion on product labels in accordance with Global Harmonized System, REACH, and any other applicable global chemical regulations. This role will interface closely with Category and Supplier Management Teams and will principally involve SDS updates, authoring new SDS as required and answering queries from global colleagues and customers. Responsibilities Generate compliant SDS using Abcam’s dedicated SDS authoring application, WERCS Maintain existing product SDS ensuring any updates to hazards and/or legislation are implemented Support management of the team dedicated inbox, where we receive customer & internal SDS requests & compliance enquiries Carry out routine governance and oversight checks, particularly for antibody, protein, peptides & lysates portfolios Provide general Regulatory Compliance Team support You will have a strong knowledge in Excel & other MS Office applications. You will have experience working with large datasets. You will have excellent attention to detail and written and verbal communication skills to resolve internal & external product data queries in a timely manner. You will have the ability to prioritise and process large amounts of data in a logical and efficient manner, ensuring our customers receive accurate data. You will be a confident individual and be able to work independently. You will hold yourself and others to high standards of accuracy and attention to detail in a fast-paced environment. Familiarity with global chemical regulations (EU CLP (Classification, Labelling and Packaging), GHS, REACH) & experience in SDS authoring would be advantageous, but not essential due to basic training being provided, as would any other experience of a previous junior regulatory affairs or product compliance role. Knowledge of the SDS authoring application WERCS would be advantageous, as would any other experience with this type of application. Qualifications You will be educated to at least degree level (or equivalent), possess a knowledge of Chemistry, Life Science, or a related field. Additional Information We know that when it comes to benefits, no one size fits all. Flexibility and choice matter which is why, in addition to market competitive salaries, we offer you a flexible benefits package which is tailored to your unique needs and support your financial, physical and emotional wellbeing. This includes 18 weeks fully paid maternity leave, 6 weeks fully paid paternity leave as well as highly flexible working and much more. Besides, your development will be integral to your experience here. You will grow alongside other talented minds, in ways you may often find unexpected. When people come together, incredible things happen. Here you’ll work in a safe environment where you can be who you truly are. We’ll champion and celebrate your uniqueness throughout your journey with us. This is how we excel at partnering with the scientific community no matter the challenge, ultimately helping solve the world’s most critical diseases. Find out more about Diversity & Inclusion at Abcam.
#J-18808-Ljbffr
